Search by Gene
| Item | Value |
|---|---|
| geneid | 23460 |
| ensemblid | ENSG00000154262.13 |
| hgncid | 36 |
| symbol | ABCA6 |
| name | ATP binding cassette subfamily A member 6 |
| refseq_nuc | NM_080284.3 |
| refseq_prot | NP_525023.2 |
| ensembl_nuc | ENST00000284425.7 |
| ensembl_prot | ENSP00000284425.1 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 69078702 |
| end | 69141895 |
| strand | - |
| ver | v1.2 |
| region | chr17:69078702-69141895 |
| region5000 | chr17:69073702-69146895 |
| regionname0 | ABCA6_chr17_69078702_69141895 |
| regionname5000 | ABCA6_chr17_69073702_69146895 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1617 | 111 | 14 | 23 | 43 | 12 | 18 | ABCA6_chr17_69073702_69146895 | ABCA6 | MNMKQ others(1612): Show |
chr17 | 69073702 | 69146895 |
| a0002 | 0/0 | 1617 | 92 | 11 | 10 | 56 | 3 | 12 | ABCA6_chr17_69073702_69146895 | ABCA6 | MNMKQ others(1612): Show |
chr17 | 69073702 | 69146895 |
| a0003 | 0/0 | 1617 | 31 | 27 | 4 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | MNMKQ others(1612): Show |
chr17 | 69073702 | 69146895 |
| a0004 | 0/0 | 1617 | 24 | 0 | 10 | 11 | 0 | 3 | ABCA6_chr17_69073702_69146895 | ABCA6 | MNMKQ others(1612): Show |
chr17 | 69073702 | 69146895 |
| a0005 | 0/0 | 1617 | 19 | 6 | 5 | 5 | 1 | 2 | ABCA6_chr17_69073702_69146895 | ABCA6 | MNMKQ others(1612): Show |
chr17 | 69073702 | 69146895 |
| a0006 | 1/0 | 1617 | 16 | 12 | 3 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | MNMKQ others(1612): Show |
chr17 | 69073702 | 69146895 |
| a0007 | 0/0 | 1617 | 9 | 7 | 0 | 2 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | MNMKQ others(1612): Show |
chr17 | 69073702 | 69146895 |
| a0008 | 0/0 | 1617 | 4 | 0 | 0 | 4 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | MNMKQ others(1612): Show |
chr17 | 69073702 | 69146895 |
| a0009 | 0/0 | 1617 | 2 | 0 | 2 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | MNMKQ others(1612): Show |
chr17 | 69073702 | 69146895 |
| a0010 | 0/0 | 1617 | 2 | 0 | 0 | 2 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | MNMKQ others(1612): Show |
chr17 | 69073702 | 69146895 |
| a0011 | 0/0 | 1617 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | MNMKQ others(1612): Show |
chr17 | 69073702 | 69146895 |
| a0012 | 0/0 | 1617 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | MNMKQ others(1612): Show |
chr17 | 69073702 | 69146895 |
| a0013 | 0/0 | 1617 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | MNMKQ others(1612): Show |
chr17 | 69073702 | 69146895 |
| a0014 | 0/0 | 1617 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | MNMKQ others(1612): Show |
chr17 | 69073702 | 69146895 |
| a0015 | 0/0 | 1617 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | MNMKQ others(1612): Show |
chr17 | 69073702 | 69146895 |
| a0016 | 0/0 | 1617 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | MNMKQ others(1612): Show |
chr17 | 69073702 | 69146895 |
| a0017 | 0/0 | 1617 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | MNMKQ others(1612): Show |
chr17 | 69073702 | 69146895 |
| a0018 | 0/0 | 1617 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | MNMKQ others(1612): Show |
chr17 | 69073702 | 69146895 |
| a0019 | 0/0 | 1617 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | MNMKQ others(1612): Show |
chr17 | 69073702 | 69146895 |
| a0020 | 0/0 | 1617 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA6_chr17_69073702_69146895 | ABCA6 | MNMKQ others(1612): Show |
chr17 | 69073702 | 69146895 |
| a0021 | 0/0 | 1617 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | MNMKQ others(1612): Show |
chr17 | 69073702 | 69146895 |
| a0022 | 0/0 | 1617 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | MNMKQ others(1612): Show |
chr17 | 69073702 | 69146895 |
| a0023 | 0/0 | 1617 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | MNMKQ others(1612): Show |
chr17 | 69073702 | 69146895 |
| a0024 | 0/0 | 1617 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | MNMKQ others(1612): Show |
chr17 | 69073702 | 69146895 |
| a0025 | 0/0 | 1617 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | MNMKQ others(1612): Show |
chr17 | 69073702 | 69146895 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 4851 | 111 | 14 | 23 | 43 | 12 | 18 | ABCA6_chr17_69073702_69146895 | ABCA6 | ATGAA others(4846): Show |
chr17 | 69073702 | 69146895 | ||
| a0002c0002 | 0/0 | 4851 | 91 | 11 | 10 | 55 | 3 | 12 | ABCA6_chr17_69073702_69146895 | ABCA6 | ATGAA others(4846): Show |
chr17 | 69073702 | 69146895 | ||
| a0002c0019 | 0/0 | 4851 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | ATGAA others(4846): Show |
chr17 | 69073702 | 69146895 | ||
| a0003c0003 | 0/0 | 4851 | 28 | 24 | 4 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | ATGAA others(4846): Show |
chr17 | 69073702 | 69146895 | ||
| a0003c0009 | 0/0 | 4851 | 3 | 3 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | ATGAA others(4846): Show |
chr17 | 69073702 | 69146895 | ||
| a0004c0004 | 0/0 | 4851 | 24 | 0 | 10 | 11 | 0 | 3 | ABCA6_chr17_69073702_69146895 | ABCA6 | ATGAA others(4846): Show |
chr17 | 69073702 | 69146895 | ||
| a0005c0005 | 0/0 | 4851 | 19 | 6 | 5 | 5 | 1 | 2 | ABCA6_chr17_69073702_69146895 | ABCA6 | ATGAA others(4846): Show |
chr17 | 69073702 | 69146895 | ||
| a0006c0007 | 0/0 | 4851 | 9 | 6 | 3 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | ATGAA others(4846): Show |
chr17 | 69073702 | 69146895 | ||
| a0006c0010 | 0/0 | 4851 | 3 | 3 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | ATGAA others(4846): Show |
chr17 | 69073702 | 69146895 | ||
| a0006c0013 | 0/0 | 4851 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | ATGAA others(4846): Show |
chr17 | 69073702 | 69146895 | ||
| a0006c0028 | 1/0 | 4851 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | ATGAA others(4846): Show |
chr17 | 69073702 | 69146895 | ||
| a0006c0031 | 0/0 | 4851 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | ATGAA others(4846): Show |
chr17 | 69073702 | 69146895 | ||
| a0007c0006 | 0/0 | 4851 | 9 | 7 | 0 | 2 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | ATGAA others(4846): Show |
chr17 | 69073702 | 69146895 | ||
| a0008c0008 | 0/0 | 4851 | 4 | 0 | 0 | 4 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | ATGAA others(4846): Show |
chr17 | 69073702 | 69146895 | ||
| a0009c0012 | 0/0 | 4851 | 2 | 0 | 2 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | ATGAA others(4846): Show |
chr17 | 69073702 | 69146895 | ||
| a0010c0014 | 0/0 | 4851 | 2 | 0 | 0 | 2 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | ATGAA others(4846): Show |
chr17 | 69073702 | 69146895 | ||
| a0011c0011 | 0/0 | 4851 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | ATGAA others(4846): Show |
chr17 | 69073702 | 69146895 | ||
| a0012c0024 | 0/0 | 4851 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | ATGAA others(4846): Show |
chr17 | 69073702 | 69146895 | ||
| a0013c0016 | 0/0 | 4851 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | ATGAA others(4846): Show |
chr17 | 69073702 | 69146895 | ||
| a0014c0021 | 0/0 | 4851 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | ATGAA others(4846): Show |
chr17 | 69073702 | 69146895 | ||
| a0015c0029 | 0/0 | 4851 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | ATGAA others(4846): Show |
chr17 | 69073702 | 69146895 | ||
| a0016c0018 | 0/0 | 4851 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | ATGAA others(4846): Show |
chr17 | 69073702 | 69146895 | ||
| a0017c0030 | 0/0 | 4851 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | ATGAA others(4846): Show |
chr17 | 69073702 | 69146895 | ||
| a0018c0022 | 0/0 | 4851 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | ATGAA others(4846): Show |
chr17 | 69073702 | 69146895 | ||
| a0019c0020 | 0/0 | 4851 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | ATGAA others(4846): Show |
chr17 | 69073702 | 69146895 | ||
| a0020c0017 | 0/0 | 4851 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA6_chr17_69073702_69146895 | ABCA6 | ATGAA others(4846): Show |
chr17 | 69073702 | 69146895 | ||
| a0021c0027 | 0/0 | 4851 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | ATGAA others(4846): Show |
chr17 | 69073702 | 69146895 | ||
| a0022c0026 | 0/0 | 4851 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | ATGAA others(4846): Show |
chr17 | 69073702 | 69146895 | ||
| a0023c0015 | 0/0 | 4851 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | ATGAA others(4846): Show |
chr17 | 69073702 | 69146895 | ||
| a0024c0023 | 0/0 | 4851 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | ATGAA others(4846): Show |
chr17 | 69073702 | 69146895 | ||
| a0025c0025 | 0/0 | 4851 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | ATGAA others(4846): Show |
chr17 | 69073702 | 69146895 |
| acthapid | grch38/chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5321 | 111 | 14 | 23 | 43 | 12 | 18 | ABCA6_chr17_69073702_69146895 | ABCA6 | AGAAA others(5316): Show |
chr17 | 69073702 | 69146895 |
| a0002c0002t0001 | 0/0 | 5321 | 4 | 3 | 1 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | AGAAA others(5316): Show |
chr17 | 69073702 | 69146895 |
| a0002c0002t0002 | 0/0 | 5321 | 86 | 8 | 9 | 54 | 3 | 12 | ABCA6_chr17_69073702_69146895 | ABCA6 | AGAAA others(5316): Show |
chr17 | 69073702 | 69146895 |
| a0002c0002t0003 | 0/0 | 5321 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | TGAAA others(5316): Show |
chr17 | 69073702 | 69146895 |
| a0002c0019t0002 | 0/0 | 5321 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | AGAAA others(5316): Show |
chr17 | 69073702 | 69146895 |
| a0003c0003t0001 | 0/0 | 5321 | 28 | 24 | 4 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | AGAAA others(5316): Show |
chr17 | 69073702 | 69146895 |
| a0003c0009t0001 | 0/0 | 5321 | 3 | 3 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | AGAAA others(5316): Show |
chr17 | 69073702 | 69146895 |
| a0004c0004t0002 | 0/0 | 5321 | 24 | 0 | 10 | 11 | 0 | 3 | ABCA6_chr17_69073702_69146895 | ABCA6 | AGAAA others(5316): Show |
chr17 | 69073702 | 69146895 |
| a0005c0005t0001 | 0/0 | 5321 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | AGAAA others(5316): Show |
chr17 | 69073702 | 69146895 |
| a0005c0005t0002 | 0/0 | 5321 | 17 | 4 | 5 | 5 | 1 | 2 | ABCA6_chr17_69073702_69146895 | ABCA6 | AGAAA others(5316): Show |
chr17 | 69073702 | 69146895 |
| a0006c0007t0001 | 0/0 | 5321 | 9 | 6 | 3 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | AGAAA others(5316): Show |
chr17 | 69073702 | 69146895 |
| a0006c0010t0001 | 0/0 | 5321 | 3 | 3 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | AGAAA others(5316): Show |
chr17 | 69073702 | 69146895 |
| a0006c0013t0001 | 0/0 | 5321 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | AGAAA others(5316): Show |
chr17 | 69073702 | 69146895 |
| a0006c0028t0002 | 1/0 | 5321 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | AGAAA others(5316): Show |
chr17 | 69073702 | 69146895 |
| a0006c0031t0001 | 0/0 | 5321 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | AGAAA others(5316): Show |
chr17 | 69073702 | 69146895 |
| a0007c0006t0001 | 0/0 | 5321 | 5 | 5 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | AGAAA others(5316): Show |
chr17 | 69073702 | 69146895 |
| a0007c0006t0002 | 0/0 | 5321 | 4 | 2 | 0 | 2 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | AGAAA others(5316): Show |
chr17 | 69073702 | 69146895 |
| a0008c0008t0002 | 0/0 | 5321 | 4 | 0 | 0 | 4 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | AGAAA others(5316): Show |
chr17 | 69073702 | 69146895 |
| a0009c0012t0002 | 0/0 | 5321 | 2 | 0 | 2 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | AGAAA others(5316): Show |
chr17 | 69073702 | 69146895 |
| a0010c0014t0002 | 0/0 | 5321 | 2 | 0 | 0 | 2 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | AGAAA others(5316): Show |
chr17 | 69073702 | 69146895 |
| a0011c0011t0001 | 0/0 | 5321 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | AGAAA others(5316): Show |
chr17 | 69073702 | 69146895 |
| a0012c0024t0002 | 0/0 | 5321 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | AGAAA others(5316): Show |
chr17 | 69073702 | 69146895 |
| a0013c0016t0001 | 0/0 | 5321 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | AGAAA others(5316): Show |
chr17 | 69073702 | 69146895 |
| a0014c0021t0001 | 0/0 | 5321 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | AGAAA others(5316): Show |
chr17 | 69073702 | 69146895 |
| a0015c0029t0001 | 0/0 | 5321 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | AGAAA others(5316): Show |
chr17 | 69073702 | 69146895 |
| a0016c0018t0002 | 0/0 | 5321 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | AGAAA others(5316): Show |
chr17 | 69073702 | 69146895 |
| a0017c0030t0002 | 0/0 | 5321 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | AGAAA others(5316): Show |
chr17 | 69073702 | 69146895 |
| a0018c0022t0001 | 0/0 | 5321 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | AGAAA others(5316): Show |
chr17 | 69073702 | 69146895 |
| a0019c0020t0001 | 0/0 | 5321 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | AGAAA others(5316): Show |
chr17 | 69073702 | 69146895 |
| a0020c0017t0001 | 0/0 | 5321 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA6_chr17_69073702_69146895 | ABCA6 | AGAAA others(5316): Show |
chr17 | 69073702 | 69146895 |
| a0021c0027t0002 | 0/0 | 5321 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | AGAAA others(5316): Show |
chr17 | 69073702 | 69146895 |
| a0022c0026t0002 | 0/0 | 5321 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | AGAAA others(5316): Show |
chr17 | 69073702 | 69146895 |
| a0023c0015t0001 | 0/0 | 5321 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | AGAAA others(5316): Show |
chr17 | 69073702 | 69146895 |
| a0024c0023t0002 | 0/0 | 5321 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | AGAAA others(5316): Show |
chr17 | 69073702 | 69146895 |
| a0025c0025t0002 | 0/0 | 5321 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | AGAAA others(5316): Show |
chr17 | 69073702 | 69146895 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 2 | 2 | 0 | 0 | 1 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0002 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0048 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0010 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0028 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0002t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0002c0019t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0003c0003t0001g0011 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0003c0003t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0003c0003t0001g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0003c0003t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0003c0003t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0003c0003t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0003c0003t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0003c0003t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0003c0003t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0003c0003t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0003c0003t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0003c0003t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0003c0003t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0003c0003t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0003c0003t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0003c0003t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0003c0003t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0003c0003t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0003c0003t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0003c0003t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0003c0003t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0003c0003t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0003c0009t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0003c0009t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0003c0009t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0004c0004t0002g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0004c0004t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0004c0004t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0004c0004t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0004c0004t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0004c0004t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0004c0004t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0004c0004t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0004c0004t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0004c0004t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0004c0004t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0004c0004t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0004c0004t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0004c0004t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0004c0004t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0004c0004t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0004c0004t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0004c0004t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0004c0004t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0004c0004t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0005c0005t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0005c0005t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0005c0005t0002g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0005c0005t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0005c0005t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0005c0005t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0005c0005t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0005c0005t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0005c0005t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0005c0005t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0005c0005t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0005c0005t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0005c0005t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0005c0005t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0005c0005t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0005c0005t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0005c0005t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0006c0007t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0006c0007t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0006c0007t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0006c0007t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0006c0007t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0006c0010t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0006c0010t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0006c0010t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0006c0013t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0006c0013t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0006c0028t0002g0227 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0006c0031t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0007c0006t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0007c0006t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0007c0006t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0007c0006t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0007c0006t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0007c0006t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0007c0006t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0007c0006t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0007c0006t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0008c0008t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0008c0008t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0008c0008t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0009c0012t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0009c0012t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0010c0014t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0010c0014t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0011c0011t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0011c0011t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0012c0024t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0013c0016t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0014c0021t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0015c0029t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0016c0018t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0017c0030t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0018c0022t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0019c0020t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0020c0017t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0021c0027t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0022c0026t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0023c0015t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0024c0023t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| a0025c0025t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0002 | g0213 | EUR | GBR | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0117 | EUR | GBR | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0101 | EUR | GBR | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG00140 | hp2 | a0002 | c0002 | t0002 | g0229 | EUR | GBR | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0122 | EUR | FIN | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG00280 | hp2 | a0002 | c0002 | t0002 | g0217 | EUR | FIN | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0179 | EUR | FIN | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0040 | EUR | FIN | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG00544 | hp2 | a0012 | c0024 | t0002 | g0215 | EAS | CHS | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG00609 | hp1 | a0004 | c0004 | t0002 | g0138 | EAS | CHS | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG00639 | hp1 | a0002 | c0002 | t0002 | g0230 | AMR | PUR | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG00639 | hp2 | a0003 | c0003 | t0001 | g0265 | AMR | PUR | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG00642 | hp2 | a0002 | c0002 | t0002 | g0220 | AMR | PUR | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG00733 | hp1 | a0005 | c0005 | t0002 | g0128 | AMR | PUR | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01069 | hp1 | a0006 | c0007 | t0001 | g0165 | AMR | PUR | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01070 | hp1 | a0005 | c0005 | t0002 | g0124 | AMR | PUR | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01071 | hp1 | a0005 | c0005 | t0002 | g0125 | AMR | PUR | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01071 | hp2 | a0006 | c0007 | t0001 | g0023 | AMR | PUR | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01074 | hp1 | a0004 | c0004 | t0002 | g0148 | AMR | PUR | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01074 | hp2 | a0002 | c0002 | t0002 | g0231 | AMR | PUR | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01099 | hp2 | a0003 | c0003 | t0001 | g0030 | AMR | PUR | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01106 | hp1 | a0006 | c0007 | t0001 | g0023 | AMR | PUR | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01109 | hp1 | a0003 | c0003 | t0001 | g0011 | AMR | PUR | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01109 | hp2 | a0002 | c0002 | t0002 | g0028 | AMR | PUR | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01167 | hp2 | a0004 | c0004 | t0002 | g0146 | AMR | PUR | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01169 | hp2 | a0004 | c0004 | t0002 | g0142 | AMR | PUR | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01192 | hp1 | a0004 | c0004 | t0002 | g0006 | AMR | PUR | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01243 | hp1 | a0005 | c0005 | t0002 | g0154 | AMR | PUR | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01243 | hp2 | a0013 | c0016 | t0001 | g0159 | AMR | PUR | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01256 | hp1 | a0002 | c0002 | t0002 | g0177 | AMR | CLM | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01258 | hp2 | a0002 | c0002 | t0002 | g0198 | AMR | CLM | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0224 | AMR | CLM | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01361 | hp1 | a0003 | c0003 | t0001 | g0278 | AMR | CLM | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01433 | hp2 | a0004 | c0004 | t0002 | g0006 | AMR | CLM | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0051 | EUR | IBS | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | IBS | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0102 | EUR | IBS | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0049 | EUR | IBS | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | IBS | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01884 | hp1 | a0006 | c0010 | t0001 | g0256 | AFR | ACB | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01884 | hp2 | a0002 | c0002 | t0002 | g0241 | AFR | ACB | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01891 | hp1 | a0005 | c0005 | t0001 | g0158 | AFR | ACB | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01891 | hp2 | a0003 | c0009 | t0001 | g0258 | AFR | ACB | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01928 | hp1 | a0002 | c0002 | t0002 | g0237 | AMR | PEL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01928 | hp2 | a0004 | c0004 | t0002 | g0006 | AMR | PEL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01934 | hp1 | a0002 | c0002 | t0002 | g0254 | AMR | PEL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01934 | hp2 | a0004 | c0004 | t0002 | g0144 | AMR | PEL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01943 | hp1 | a0004 | c0004 | t0002 | g0143 | AMR | PEL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01952 | hp1 | a0004 | c0004 | t0002 | g0145 | AMR | PEL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01975 | hp2 | a0009 | c0012 | t0002 | g0139 | AMR | PEL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01978 | hp2 | a0004 | c0004 | t0002 | g0147 | AMR | PEL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02004 | hp2 | a0009 | c0012 | t0002 | g0137 | AMR | PEL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02015 | hp1 | a0004 | c0004 | t0002 | g0130 | EAS | KHV | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02015 | hp2 | a0002 | c0002 | t0002 | g0206 | EAS | KHV | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02040 | hp1 | a0005 | c0005 | t0002 | g0007 | EAS | KHV | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02040 | hp2 | a0010 | c0014 | t0002 | g0247 | EAS | KHV | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0169 | AFR | ACB | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02055 | hp2 | a0003 | c0003 | t0001 | g0273 | AFR | ACB | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02071 | hp1 | a0005 | c0005 | t0002 | g0126 | EAS | KHV | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02071 | hp2 | a0002 | c0002 | t0002 | g0200 | EAS | KHV | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02074 | hp2 | a0002 | c0002 | t0002 | g0201 | EAS | KHV | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0194 | EAS | KHV | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02135 | hp2 | a0002 | c0002 | t0002 | g0178 | EAS | KHV | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02145 | hp2 | a0006 | c0013 | t0001 | g0246 | AFR | ACB | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02148 | hp2 | a0005 | c0005 | t0002 | g0155 | AMR | PEL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02165 | hp1 | a0002 | c0002 | t0002 | g0182 | EAS | CDX | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CDX | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02257 | hp1 | a0007 | c0006 | t0001 | g0061 | AFR | ACB | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02257 | hp2 | a0003 | c0003 | t0001 | g0032 | AFR | ACB | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02280 | hp1 | a0002 | c0002 | t0001 | g0025 | AFR | ACB | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02451 | hp1 | a0003 | c0003 | t0001 | g0267 | AFR | ACB | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02451 | hp2 | a0003 | c0009 | t0001 | g0167 | AFR | ACB | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02523 | hp1 | a0002 | c0002 | t0002 | g0244 | EAS | KHV | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02523 | hp2 | a0002 | c0002 | t0002 | g0205 | EAS | KHV | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02572 | hp1 | a0003 | c0003 | t0001 | g0269 | AFR | GWD | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02602 | hp2 | a0002 | c0002 | t0002 | g0172 | SAS | PJL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02622 | hp1 | a0015 | c0029 | t0001 | g0240 | AFR | GWD | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02622 | hp2 | a0016 | c0018 | t0002 | g0060 | AFR | GWD | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02630 | hp1 | a0003 | c0003 | t0001 | g0262 | AFR | GWD | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02630 | hp2 | a0003 | c0003 | t0001 | g0276 | AFR | GWD | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02647 | hp1 | a0006 | c0007 | t0001 | g0008 | AFR | GWD | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02698 | hp2 | a0002 | c0002 | t0002 | g0232 | SAS | PJL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02717 | hp1 | a0006 | c0007 | t0001 | g0008 | AFR | GWD | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02723 | hp1 | a0007 | c0006 | t0001 | g0105 | AFR | GWD | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02723 | hp2 | a0003 | c0003 | t0001 | g0264 | AFR | GWD | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02735 | hp1 | a0002 | c0002 | t0002 | g0028 | SAS | PJL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02809 | hp2 | a0003 | c0003 | t0001 | g0259 | AFR | GWD | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02818 | hp1 | a0003 | c0003 | t0001 | g0012 | AFR | GWD | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02818 | hp2 | a0002 | c0002 | t0002 | g0242 | AFR | GWD | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02886 | hp1 | a0003 | c0003 | t0001 | g0266 | AFR | GWD | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02886 | hp2 | a0005 | c0005 | t0002 | g0132 | AFR | GWD | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02895 | hp1 | a0003 | c0003 | t0001 | g0031 | AFR | GWD | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02895 | hp2 | a0017 | c0030 | t0002 | g0129 | AFR | GWD | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02922 | hp1 | a0006 | c0007 | t0001 | g0164 | AFR | ESN | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02922 | hp2 | a0002 | c0002 | t0002 | g0253 | AFR | ESN | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02965 | hp1 | a0003 | c0003 | t0001 | g0277 | AFR | ESN | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ESN | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02970 | hp1 | a0006 | c0013 | t0001 | g0163 | AFR | ESN | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG03041 | hp1 | a0003 | c0003 | t0001 | g0260 | AFR | GWD | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG03041 | hp2 | a0007 | c0006 | t0002 | g0110 | AFR | GWD | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG03098 | hp1 | a0011 | c0011 | t0001 | g0044 | AFR | MSL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG03098 | hp2 | a0003 | c0003 | t0001 | g0012 | AFR | MSL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG03130 | hp1 | a0018 | c0022 | t0001 | g0272 | AFR | ESN | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG03130 | hp2 | a0002 | c0002 | t0002 | g0243 | AFR | ESN | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG03139 | hp1 | a0007 | c0006 | t0002 | g0035 | AFR | ESN | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG03139 | hp2 | a0002 | c0002 | t0002 | g0233 | AFR | ESN | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG03195 | hp1 | a0003 | c0003 | t0001 | g0261 | AFR | ESN | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG03209 | hp1 | a0005 | c0005 | t0002 | g0160 | AFR | MSL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG03209 | hp2 | a0019 | c0020 | t0001 | g0263 | AFR | MSL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG03225 | hp1 | a0006 | c0010 | t0001 | g0257 | AFR | MSL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG03225 | hp2 | a0003 | c0003 | t0001 | g0268 | AFR | MSL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG03239 | hp1 | a0020 | c0017 | t0001 | g0100 | SAS | PJL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG03453 | hp1 | a0003 | c0003 | t0001 | g0274 | AFR | MSL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG03453 | hp2 | a0005 | c0005 | t0001 | g0157 | AFR | MSL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG03486 | hp1 | a0007 | c0006 | t0001 | g0088 | AFR | MSL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG03486 | hp2 | a0003 | c0003 | t0001 | g0011 | AFR | MSL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG03490 | hp1 | a0002 | c0002 | t0002 | g0029 | SAS | PJL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG03490 | hp2 | a0005 | c0005 | t0002 | g0127 | SAS | PJL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG03492 | hp2 | a0002 | c0002 | t0002 | g0029 | SAS | PJL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG03516 | hp1 | a0011 | c0011 | t0001 | g0043 | AFR | ESN | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG03516 | hp2 | a0003 | c0009 | t0001 | g0168 | AFR | ESN | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG03579 | hp1 | a0003 | c0003 | t0001 | g0270 | AFR | MSL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG03579 | hp2 | a0006 | c0031 | t0001 | g0252 | AFR | MSL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG03654 | hp1 | a0002 | c0002 | t0002 | g0238 | SAS | PJL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | STU | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG03688 | hp2 | a0002 | c0002 | t0002 | g0190 | SAS | STU | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG03704 | hp1 | a0005 | c0005 | t0002 | g0152 | SAS | PJL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG03834 | hp1 | a0002 | c0002 | t0002 | g0199 | SAS | BEB | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG03834 | hp2 | a0004 | c0004 | t0002 | g0141 | SAS | BEB | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG03942 | hp1 | a0002 | c0002 | t0002 | g0181 | SAS | BEB | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | BEB | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG04115 | hp1 | a0004 | c0004 | t0002 | g0140 | SAS | STU | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | STU | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | BEB | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG04184 | hp2 | a0002 | c0002 | t0002 | g0226 | SAS | BEB | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | STU | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG04199 | hp2 | a0004 | c0004 | t0002 | g0149 | SAS | STU | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG04204 | hp2 | a0002 | c0002 | t0002 | g0166 | SAS | STU | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18522 | hp1 | a0002 | c0002 | t0002 | g0245 | AFR | YRI | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18522 | hp2 | a0003 | c0003 | t0001 | g0011 | AFR | YRI | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18612 | hp1 | a0004 | c0004 | t0002 | g0033 | EAS | CHB | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18612 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | CHB | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18940 | hp1 | a0002 | c0002 | t0002 | g0175 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18940 | hp2 | a0005 | c0005 | t0002 | g0007 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18942 | hp2 | a0002 | c0002 | t0002 | g0192 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18945 | hp1 | a0004 | c0004 | t0002 | g0021 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18945 | hp2 | a0002 | c0002 | t0002 | g0219 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18948 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18948 | hp2 | a0022 | c0026 | t0002 | g0106 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18952 | hp1 | a0007 | c0006 | t0002 | g0057 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18953 | hp1 | a0002 | c0002 | t0002 | g0212 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18957 | hp2 | a0002 | c0002 | t0002 | g0027 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18959 | hp1 | a0005 | c0005 | t0002 | g0007 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18959 | hp2 | a0002 | c0002 | t0002 | g0211 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18962 | hp2 | a0002 | c0002 | t0003 | g0228 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18963 | hp1 | a0002 | c0002 | t0002 | g0026 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18965 | hp2 | a0004 | c0004 | t0002 | g0135 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18967 | hp2 | a0002 | c0002 | t0002 | g0197 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18969 | hp1 | a0002 | c0002 | t0002 | g0027 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18971 | hp2 | a0002 | c0002 | t0002 | g0183 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18973 | hp2 | a0002 | c0002 | t0002 | g0234 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18974 | hp1 | a0008 | c0008 | t0002 | g0020 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18974 | hp2 | a0002 | c0002 | t0002 | g0204 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18977 | hp1 | a0002 | c0002 | t0002 | g0189 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18982 | hp1 | a0002 | c0002 | t0002 | g0223 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18985 | hp1 | a0002 | c0002 | t0002 | g0209 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18985 | hp2 | a0008 | c0008 | t0002 | g0134 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18987 | hp2 | a0002 | c0002 | t0002 | g0162 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18989 | hp1 | a0002 | c0002 | t0002 | g0195 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18989 | hp2 | a0004 | c0004 | t0002 | g0022 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18993 | hp1 | a0002 | c0002 | t0002 | g0216 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18993 | hp2 | a0008 | c0008 | t0002 | g0020 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19000 | hp1 | a0004 | c0004 | t0002 | g0153 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19000 | hp2 | a0002 | c0002 | t0002 | g0203 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19001 | hp2 | a0002 | c0002 | t0002 | g0191 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19002 | hp2 | a0004 | c0004 | t0002 | g0022 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19004 | hp2 | a0002 | c0002 | t0002 | g0187 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19006 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19007 | hp2 | a0002 | c0002 | t0002 | g0196 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19010 | hp1 | a0002 | c0002 | t0002 | g0184 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19030 | hp1 | a0006 | c0010 | t0001 | g0255 | AFR | LWK | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19030 | hp2 | a0005 | c0005 | t0002 | g0131 | AFR | LWK | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19043 | hp1 | a0002 | c0002 | t0002 | g0193 | AFR | LWK | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19043 | hp2 | a0006 | c0007 | t0001 | g0024 | AFR | LWK | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19054 | hp2 | a0002 | c0002 | t0002 | g0248 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19060 | hp1 | a0005 | c0005 | t0002 | g0151 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19062 | hp1 | a0002 | c0002 | t0002 | g0171 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19063 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19064 | hp1 | a0002 | c0002 | t0002 | g0251 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19065 | hp2 | a0002 | c0002 | t0002 | g0208 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19066 | hp1 | a0023 | c0015 | t0001 | g0047 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19066 | hp2 | a0002 | c0002 | t0002 | g0236 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19068 | hp1 | a0004 | c0004 | t0002 | g0021 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19068 | hp2 | a0002 | c0002 | t0002 | g0221 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19070 | hp2 | a0002 | c0002 | t0002 | g0225 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19072 | hp1 | a0004 | c0004 | t0002 | g0150 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19072 | hp2 | a0002 | c0002 | t0002 | g0214 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19074 | hp1 | a0004 | c0004 | t0002 | g0136 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19074 | hp2 | a0002 | c0002 | t0002 | g0210 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19075 | hp2 | a0002 | c0002 | t0002 | g0185 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19078 | hp1 | a0002 | c0002 | t0002 | g0173 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19081 | hp2 | a0002 | c0002 | t0002 | g0176 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19082 | hp1 | a0002 | c0019 | t0002 | g0186 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19083 | hp1 | a0002 | c0002 | t0002 | g0207 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19084 | hp1 | a0002 | c0002 | t0002 | g0170 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19084 | hp2 | a0002 | c0002 | t0002 | g0239 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19085 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19086 | hp1 | a0010 | c0014 | t0002 | g0250 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19086 | hp2 | a0008 | c0008 | t0002 | g0133 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19087 | hp1 | a0007 | c0006 | t0002 | g0099 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19087 | hp2 | a0002 | c0002 | t0002 | g0235 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19089 | hp1 | a0024 | c0023 | t0002 | g0188 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19090 | hp1 | a0002 | c0002 | t0002 | g0174 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19091 | hp2 | a0025 | c0025 | t0002 | g0249 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19240 | hp1 | a0003 | c0003 | t0001 | g0031 | AFR | YRI | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | YRI | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA20129 | hp1 | a0006 | c0007 | t0001 | g0008 | AFR | ASW | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | TSI | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA20752 | hp2 | a0005 | c0005 | t0002 | g0156 | EUR | TSI | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA20905 | hp2 | a0002 | c0002 | t0002 | g0218 | SAS | GIH | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG01123 | hp2 | a0002 | c0002 | t0002 | g0010 | AMR | CLM | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02109 | hp2 | a0007 | c0006 | t0001 | g0087 | AFR | ACB | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02486 | hp1 | a0002 | c0002 | t0002 | g0222 | AFR | ACB | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02486 | hp2 | a0014 | c0021 | t0001 | g0271 | AFR | ACB | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG02559 | hp2 | a0003 | c0003 | t0001 | g0030 | AFR | ACB | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0025 | AFR | MSL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG03471 | hp2 | a0006 | c0007 | t0001 | g0024 | AFR | MSL | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG06807 | hp1 | a0021 | c0027 | t0002 | g0202 | AFR | USA | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| HG06807 | hp2 | a0003 | c0003 | t0001 | g0012 | AFR | USA | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA18955 | hp2 | a0002 | c0002 | t0002 | g0026 | EAS | JPT | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA20300 | hp1 | a0003 | c0003 | t0001 | g0275 | AFR | USA | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | USA | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA21309 | hp1 | a0005 | c0005 | t0002 | g0123 | AFR | LWK | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| NA21309 | hp2 | a0007 | c0006 | t0001 | g0104 | AFR | LWK | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0048 | REF | REF | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| homoSapiens | grch38p0 | a0006 | c0028 | t0002 | g0227 | REF | REF | ABCA6_chr17_69073702_69146895 | ABCA6 | chr17 | 69073702 | 69146895 |
| view | chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:69081069 | C | T | 1 | a0012 | 1 | HG00544.hp2 | missense_variant | MODERATE | c.4693G>A | p.Ala1565Thr | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 37/39 | 4889/5321 | 4693/4854 | 1565/1617 | chr17 | 69081069 | |||
| chr17:69081096 | G | T | 1 | a0009 | 2 | HG01975.hp2 HG02004.hp2 |
missense_variant | MODERATE | c.4666C>A | p.Leu1556Ile | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 37/39 | 4862/5321 | 4666/4854 | 1556/1617 | chr17 | 69081096 | |||
| chr17:69083300 | C | G | 1 | a0010 | 2 | HG02040.hp2 NA19086.hp1 |
missense_variant | MODERATE | c.4387G>C | p.Glu1463Gln | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 35/39 | 4583/5321 | 4387/4854 | 1463/1617 | chr17 | 69083300 | |||
| chr17:69084301 | G | A | 1 | a0014 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.4315C>T | p.Pro1439Ser | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 34/39 | 4511/5321 | 4315/4854 | 1439/1617 | chr17 | 69084301 | |||
| chr17:69085107 | G | C | 1 | a0025 | 1 | NA19091.hp2 | missense_variant | MODERATE | c.4105C>G | p.Leu1369Val | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 32/39 | 4301/5321 | 4105/4854 | 1369/1617 | chr17 | 69085107 | |||
| chr17:69085689 | T | C | 7 | a0001a0004a0008others(4): Show | 143 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(140): Show |
missense_variant | MODERATE | c.3965A>G | p.Asn1322Ser | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 31/39 | 4161/5321 | 3965/4854 | 1322/1617 | chr17 | 69085689 | |||
| chr17:69086729 | C | T | 1 | a0011 | 2 | HG03098.hp1 HG03516.hp1 |
missense_variant | MODERATE | c.3826G>A | p.Val1276Ile | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 30/39 | 4022/5321 | 3826/4854 | 1276/1617 | chr17 | 69086729 | |||
| chr17:69087355 | C | T | 1 | a0016 | 1 | HG02622.hp2 | missense_variant&splice_region_variant | MODERATE | c.3817G>A | p.Glu1273Lys | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 29/39 | 4013/5321 | 3817/4854 | 1273/1617 | chr17 | 69087355 | |||
| chr17:69088219 | A | C | 1 | a0020 | 1 | HG03239.hp1 | missense_variant | MODERATE | c.3646T>G | p.Cys1216Gly | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 28/39 | 3842/5321 | 3646/4854 | 1216/1617 | chr17 | 69088219 | |||
| chr17:69096764 | T | C | 1 | a0018 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.3158A>G | p.Tyr1053Cys | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 24/39 | 3354/5321 | 3158/4854 | 1053/1617 | chr17 | 69096764 | |||
| chr17:69096788 | G | A | 1 | a0021 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.3134C>T | p.Ser1045Phe | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 24/39 | 3330/5321 | 3134/4854 | 1045/1617 | chr17 | 69096788 | |||
| chr17:69105577 | C | T | 12 | a0001a0002a0007others(9): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
missense_variant | MODERATE | c.2625G>A | p.Met875Ile | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 20/39 | 2821/5321 | 2625/4854 | 875/1617 | chr17 | 69105577 | |||
| chr17:69106192 | C | G | 1 | a0019 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.2409G>C | p.Met803Ile | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 19/39 | 2605/5321 | 2409/4854 | 803/1617 | chr17 | 69106192 | |||
| chr17:69110801 | C | T | 1 | a0024 | 1 | NA19089.hp1 | missense_variant&splice_region_variant | MODERATE | c.2272G>A | p.Asp758Asn | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 17/39 | 2468/5321 | 2272/4854 | 758/1617 | chr17 | 69110801 | |||
| chr17:69112221 | C | G | 11 | a0003a0004a0005others(8): Show | 87 | HG00609.hp1 HG00639.hp2 HG00733.hp1 others(84): Show |
missense_variant | MODERATE | c.2094G>C | p.Met698Ile | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 16/39 | 2290/5321 | 2094/4854 | 698/1617 | chr17 | 69112221 | |||
| chr17:69113692 | T | A | 7 | a0004a0005a0008others(4): Show | 53 | HG00609.hp1 HG00733.hp1 HG01070.hp1 others(50): Show |
missense_variant | MODERATE | c.1828A>T | p.Asn610Tyr | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 14/39 | 2024/5321 | 1828/4854 | 610/1617 | chr17 | 69113692 | |||
| chr17:69115434 | A | T | 1 | a0013 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.1548T>A | p.Ser516Arg | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 12/39 | 1744/5321 | 1548/4854 | 516/1617 | chr17 | 69115434 | |||
| chr17:69124968 | A | G | 1 | a0008 | 4 | NA18974.hp1 NA18985.hp2 NA18993.hp2 others(1): Show |
missense_variant | MODERATE | c.1187T>C | p.Met396Thr | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 9/39 | 1383/5321 | 1187/4854 | 396/1617 | chr17 | 69124968 | |||
| chr17:69129699 | C | T | 12 | a0001a0004a0005others(9): Show | 175 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(172): Show |
missense_variant | MODERATE | c.844G>A | p.Val282Ile | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 7/39 | 1040/5321 | 844/4854 | 282/1617 | chr17 | 69129699 | |||
| chr17:69133710 | T | C | 1 | a0015 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.722A>G | p.Asn241Ser | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 6/39 | 918/5321 | 722/4854 | 241/1617 | chr17 | 69133710 | |||
| chr17:69133840 | C | G | 1 | a0023 | 1 | NA19066.hp1 | missense_variant | MODERATE | c.592G>C | p.Glu198Gln | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 6/39 | 788/5321 | 592/4854 | 198/1617 | chr17 | 69133840 | |||
| chr17:69134707 | T | C | 1 | a0017 | 1 | HG02895.hp2 | missense_variant | MODERATE | c.496A>G | p.Thr166Ala | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 5/39 | 692/5321 | 496/4854 | 166/1617 | chr17 | 69134707 |
| view | chr:pos | ref | alt | # # of chapid
|
chapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:69083313 | G | A | 3 | a0003c0009a0006c0007a0006c0010 | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
synonymous_variant | LOW | c.4374C>T | p.Val1458Val | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 35/39 | 4570/5321 | 4374/4854 | 1458/1617 | chr17 | 69083313 | |||
| chr17:69086718 | G | A | 1 | a0006c0013 | 2 | HG02145.hp2 HG02970.hp1 |
synonymous_variant | LOW | c.3837C>T | p.Ala1279Ala | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 30/39 | 4033/5321 | 3837/4854 | 1279/1617 | chr17 | 69086718 | |||
| chr17:69091215 | T | C | 1 | a0006c0007 | 9 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(6): Show |
synonymous_variant | LOW | c.3456A>G | p.Leu1152Leu | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 26/39 | 3652/5321 | 3456/4854 | 1152/1617 | chr17 | 69091215 | |||
| chr17:69096784 | C | T | 1 | a0006c0013 | 2 | HG02145.hp2 HG02970.hp1 |
synonymous_variant | LOW | c.3138G>A | p.Gln1046Gln | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 24/39 | 3334/5321 | 3138/4854 | 1046/1617 | chr17 | 69096784 | |||
| chr17:69113352 | A | G | 7 | a0003c0003a0003c0009a0006c0013others(4): Show | 37 | HG00639.hp2 HG01099.hp2 HG01109.hp1 others(34): Show |
synonymous_variant | LOW | c.1911T>C | p.Leu637Leu | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 15/39 | 2107/5321 | 1911/4854 | 637/1617 | chr17 | 69113352 | |||
| chr17:69114822 | C | T | 1 | a0002c0019 | 1 | NA19082.hp1 | synonymous_variant | LOW | c.1722G>A | p.Lys574Lys | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 13/39 | 1918/5321 | 1722/4854 | 574/1617 | chr17 | 69114822 | |||
| chr17:69136210 | G | A | 1 | a0006c0031 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.342C>T | p.Asp114Asp | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 4/39 | 538/5321 | 342/4854 | 114/1617 | chr17 | 69136210 |
| view | chr:pos | ref | alt | # # of thapid:transcript level
|
thapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:69078931 | G | A | 18 | a0001c0001t0001a0002c0002t0001a0003c0003t0001others(15): Show | 176 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(173): Show |
3_prime_UTR_variant | MODIFIER | c.*42C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 39/39 | 42 | chr17 | 69078931 | ||||||
| chr17:69141895 | T | A | 1 | a0002c0002t0003 | 1 | NA18962.hp2 | 5_prime_UTR_variant | MODIFIER | c.-196A>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 1/39 | 1192 | chr17 | 69141895 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level
|
ghapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:69079153 | C | T | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(189): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.4752+57G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 38/38 | chr17 | 69079153 | |||||||
| chr17:69079202 | T | C | 1 | a0015c0029t0001g0240 | 1 | HG02622.hp1 | splice_region_variant&intron_variant | LOW | c.4752+8A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 38/38 | chr17 | 69079202 | |||||||
| chr17:69079375 | T | C | 30 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0030others(27): Show | 36 | HG00639.hp2 HG01099.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.4697-110A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 37/38 | chr17 | 69079375 | |||||||
| chr17:69079508 | G | A | 5 | a0006c0007t0001g0008a0006c0007t0001g0023a0006c0007t0001g0024others(2): Show | 9 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.4697-243C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 37/38 | chr17 | 69079508 | |||||||
| chr17:69079750 | A | G | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(202): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.4697-485T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 37/38 | chr17 | 69079750 | |||||||
| chr17:69080514 | C | T | 1 | a0001c0001t0001g0019 | 2 | NA18955.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.4696+552G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 37/38 | chr17 | 69080514 | |||||||
| chr17:69080781 | C | T | 1 | a0002c0002t0002g0214 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.4696+285G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 37/38 | chr17 | 69080781 | |||||||
| chr17:69080944 | T | G | 2 | a0006c0013t0001g0163a0006c0013t0001g0246 | 2 | HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.4696+122A>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 37/38 | chr17 | 69080944 | |||||||
| chr17:69081332 | C | T | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(189): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.4617-187G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 36/38 | chr17 | 69081332 | |||||||
| chr17:69081391 | G | A | 1 | a0007c0006t0002g0099 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.4617-246C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 36/38 | chr17 | 69081391 | |||||||
| chr17:69081441 | G | T | 6 | a0003c0009t0001g0167a0003c0009t0001g0168a0003c0009t0001g0258others(3): Show | 6 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.4617-296C>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 36/38 | chr17 | 69081441 | |||||||
| chr17:69081546 | C | T | 1 | a0003c0003t0001g0273 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4617-401G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 36/38 | chr17 | 69081546 | |||||||
| chr17:69081589 | A | C | 2 | a0002c0002t0002g0245a0007c0006t0002g0110 | 2 | HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.4617-444T>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 36/38 | chr17 | 69081589 | |||||||
| chr17:69081653 | G | A | 11 | a0003c0009t0001g0167a0003c0009t0001g0168a0003c0009t0001g0258others(8): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.4617-508C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 36/38 | chr17 | 69081653 | |||||||
| chr17:69081664 | C | T | 2 | a0001c0001t0001g0037a0001c0001t0001g0075 | 2 | HG02717.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.4617-519G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 36/38 | chr17 | 69081664 | |||||||
| chr17:69081811 | T | G | 5 | a0001c0001t0001g0034a0001c0001t0001g0056a0001c0001t0001g0064others(2): Show | 5 | NA18973.hp1 NA19002.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.4617-666A>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 36/38 | chr17 | 69081811 | |||||||
| chr17:69082010 | G | A | 1 | a0006c0013t0001g0246 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.4616+863C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 36/38 | chr17 | 69082010 | |||||||
| chr17:69082328 | A | AAC | 12 | a0002c0002t0002g0166a0002c0002t0002g0175a0002c0002t0002g0178others(9): Show | 12 | HG00140.hp2 HG00639.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.4616+543_4616+544d others(4): Show |
ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 36/38 | chr17 | 69082328 | |||||||
| chr17:69082328 | AAC | A | 54 | a0001c0001t0001g0119a0002c0002t0002g0176a0002c0002t0002g0189others(51): Show | 65 | HG00609.hp1 HG00733.hp1 HG01069.hp1 others(62): Show |
intron_variant | MODIFIER | c.4616+543_4616+544d others(4): Show |
ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 36/38 | chr17 | 69082328 | |||||||
| chr17:69082328 | AACAC | A | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(112): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.4616+541_4616+544d others(6): Show |
ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 36/38 | chr17 | 69082328 | |||||||
| chr17:69082328 | AACACAC | A | 8 | a0001c0001t0001g0046a0001c0001t0001g0089a0001c0001t0001g0090others(5): Show | 8 | HG01069.hp2 HG02559.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.4616+539_4616+544d others(8): Show |
ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 36/38 | chr17 | 69082328 | |||||||
| chr17:69082328 | AACACACA others(9): Show |
A | 2 | a0006c0013t0001g0163a0006c0013t0001g0246 | 2 | HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.4616+529_4616+544d others(18): Show |
ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 36/38 | chr17 | 69082328 | |||||||
| chr17:69082459 | C | T | 1 | a0006c0013t0001g0246 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.4616+414G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 36/38 | chr17 | 69082459 | |||||||
| chr17:69082469 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.4616+404T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 36/38 | chr17 | 69082469 | |||||||
| chr17:69082543 | G | A | 101 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(98): Show | 123 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.4616+330C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 36/38 | chr17 | 69082543 | |||||||
| chr17:69082575 | T | C | 11 | a0003c0003t0001g0030a0003c0003t0001g0031a0003c0003t0001g0032others(8): Show | 13 | HG01099.hp2 HG02055.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.4616+298A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 36/38 | chr17 | 69082575 | |||||||
| chr17:69082665 | A | G | 114 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(111): Show | 140 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.4616+208T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 36/38 | chr17 | 69082665 | |||||||
| chr17:69082735 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.4616+138T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 36/38 | chr17 | 69082735 | |||||||
| chr17:69082770 | T | G | 2 | a0006c0013t0001g0163a0006c0013t0001g0246 | 2 | HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.4616+103A>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 36/38 | chr17 | 69082770 | |||||||
| chr17:69083211 | C | T | 1 | a0002c0002t0002g0223 | 1 | NA18982.hp1 | splice_donor_variant&intron_variant | HIGH | c.4475+1G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 35/38 | chr17 | 69083211 | |||||||
| chr17:69083756 | G | C | 1 | a0006c0013t0001g0163 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.4356-425C>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 34/38 | chr17 | 69083756 | |||||||
| chr17:69083850 | G | A | 1 | a0013c0016t0001g0159 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.4355+411C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 34/38 | chr17 | 69083850 | |||||||
| chr17:69084424 | G | A | 3 | a0001c0001t0001g0075a0006c0013t0001g0163a0006c0013t0001g0246 | 3 | HG02145.hp2 HG02717.hp2 HG02970.hp1 |
splice_region_variant&intron_variant | LOW | c.4260+8C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 33/38 | chr17 | 69084424 | |||||||
| chr17:69084629 | A | G | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(142): Show | 177 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.4185-122T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 32/38 | chr17 | 69084629 | |||||||
| chr17:69084670 | C | CT | 30 | a0002c0002t0002g0254a0003c0003t0001g0011a0003c0003t0001g0012others(27): Show | 36 | HG00639.hp2 HG01099.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.4185-164dupA | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 32/38 | chr17 | 69084670 | |||||||
| chr17:69084670 | CT | C | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(95): Show | 119 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.4185-164delA | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 32/38 | chr17 | 69084670 | |||||||
| chr17:69084843 | T | G | 64 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(61): Show | 83 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.4184+185A>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 32/38 | chr17 | 69084843 | |||||||
| chr17:69084874 | A | T | 1 | a0001c0001t0001g0121 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.4184+154T>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 32/38 | chr17 | 69084874 | |||||||
| chr17:69084989 | T | A | 11 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(8): Show | 11 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(8): Show |
intron_variant | MODIFIER | c.4184+39A>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 32/38 | chr17 | 69084989 | |||||||
| chr17:69085020 | G | A | 3 | a0002c0002t0002g0229a0002c0002t0002g0230a0002c0002t0002g0231 | 3 | HG00140.hp2 HG00639.hp1 HG01074.hp2 |
splice_region_variant&intron_variant | LOW | c.4184+8C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 32/38 | chr17 | 69085020 | |||||||
| chr17:69085269 | A | C | 2 | a0002c0002t0001g0025a0002c0002t0001g0169 | 3 | HG02055.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4030-87T>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 31/38 | chr17 | 69085269 | |||||||
| chr17:69085281 | C | A | 2 | a0003c0009t0001g0167a0003c0009t0001g0258 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.4030-99G>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 31/38 | chr17 | 69085281 | |||||||
| chr17:69085372 | A | G | 114 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(111): Show | 140 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.4030-190T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 31/38 | chr17 | 69085372 | |||||||
| chr17:69085502 | T | C | 3 | a0006c0010t0001g0255a0006c0010t0001g0256a0006c0010t0001g0257 | 3 | HG01884.hp1 HG03225.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.4029+123A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 31/38 | chr17 | 69085502 | |||||||
| chr17:69085519 | C | CA | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(112): Show | 136 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.4029+105dupT | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 31/38 | chr17 | 69085519 | |||||||
| chr17:69085519 | C | CAAA | 7 | a0006c0007t0001g0008a0006c0007t0001g0023a0006c0007t0001g0024others(4): Show | 11 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.4029+103_4029+105d others(5): Show |
ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 31/38 | chr17 | 69085519 | |||||||
| chr17:69085531 | A | G | 1 | a0013c0016t0001g0159 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.4029+94T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 31/38 | chr17 | 69085531 | |||||||
| chr17:69085591 | C | T | 114 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(111): Show | 140 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.4029+34G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 31/38 | chr17 | 69085591 | |||||||
| chr17:69085735 | C | T | 1 | a0004c0004t0002g0144 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.3938-19G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 30/38 | chr17 | 69085735 | |||||||
| chr17:69085856 | G | A | 1 | a0015c0029t0001g0240 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3938-140C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 30/38 | chr17 | 69085856 | |||||||
| chr17:69085921 | G | T | 2 | a0011c0011t0001g0043a0011c0011t0001g0044 | 2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3938-205C>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 30/38 | chr17 | 69085921 | |||||||
| chr17:69085943 | T | C | 1 | a0003c0003t0001g0268 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3938-227A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 30/38 | chr17 | 69085943 | |||||||
| chr17:69086125 | G | A | 91 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0026others(88): Show | 99 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.3938-409C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 30/38 | chr17 | 69086125 | |||||||
| chr17:69086226 | A | G | 2 | a0002c0002t0001g0025a0002c0002t0001g0169 | 3 | HG02055.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3937+392T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 30/38 | chr17 | 69086226 | |||||||
| chr17:69086301 | C | T | 2 | a0006c0013t0001g0163a0006c0013t0001g0246 | 2 | HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3937+317G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 30/38 | chr17 | 69086301 | |||||||
| chr17:69086486 | A | AAT | 10 | a0001c0001t0001g0013a0001c0001t0001g0098a0003c0009t0001g0167others(7): Show | 13 | HG01516.hp1 HG01517.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.3937+130_3937+131d others(4): Show |
ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 30/38 | chr17 | 69086486 | |||||||
| chr17:69086486 | A | AATATAT | 20 | a0002c0002t0002g0010a0002c0002t0002g0028a0002c0002t0002g0029others(17): Show | 29 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.3937+126_3937+131d others(8): Show |
ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 30/38 | chr17 | 69086486 | |||||||
| chr17:69086486 | A | AATATATA others(1): Show |
22 | a0002c0002t0002g0026a0002c0002t0002g0173a0002c0002t0002g0176others(19): Show | 23 | HG00099.hp1 HG00280.hp2 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.3937+124_3937+131d others(10): Show |
ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 30/38 | chr17 | 69086486 | |||||||
| chr17:69086486 | A | AATATATA others(3): Show |
4 | a0002c0002t0002g0248a0016c0018t0002g0060a0021c0027t0002g0202others(1): Show | 4 | HG02622.hp2 HG06807.hp1 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.3937+122_3937+131d others(12): Show |
ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 30/38 | chr17 | 69086486 | |||||||
| chr17:69086486 | A | AATATATA others(5): Show |
5 | a0002c0002t0002g0189a0002c0002t0002g0238a0002c0002t0002g0245others(2): Show | 5 | HG03041.hp2 HG03139.hp1 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.3937+120_3937+131d others(14): Show |
ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 30/38 | chr17 | 69086486 | |||||||
| chr17:69086486 | A | AATATATA others(7): Show |
5 | a0002c0002t0002g0197a0002c0002t0002g0226a0002c0002t0002g0242others(2): Show | 5 | HG00544.hp2 HG02818.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.3937+118_3937+131d others(16): Show |
ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 30/38 | chr17 | 69086486 | |||||||
| chr17:69086486 | A | AATATATA others(9): Show |
7 | a0002c0002t0002g0171a0002c0002t0002g0175a0002c0002t0002g0183others(4): Show | 7 | HG02523.hp1 NA18940.hp1 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.3937+116_3937+131d others(18): Show |
ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 30/38 | chr17 | 69086486 | |||||||
| chr17:69086486 | A | AATATATA others(11): Show |
4 | a0002c0002t0002g0174a0002c0002t0002g0181a0002c0002t0002g0187others(1): Show | 4 | HG03942.hp1 NA19004.hp2 NA19087.hp2 others(1): Show |
intron_variant | MODIFIER | c.3937+114_3937+131d others(20): Show |
ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 30/38 | chr17 | 69086486 | |||||||
| chr17:69086486 | A | AATATATA others(13): Show |
8 | a0002c0002t0002g0178a0002c0002t0002g0192a0002c0002t0002g0196others(5): Show | 8 | HG01884.hp2 HG02135.hp2 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.3937+112_3937+131d others(22): Show |
ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 30/38 | chr17 | 69086486 | |||||||
| chr17:69086486 | A | AATATATA others(15): Show |
4 | a0002c0002t0002g0195a0002c0002t0002g0212a0002c0019t0002g0186others(1): Show | 4 | HG02970.hp1 NA18953.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.3937+110_3937+131d others(24): Show |
ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 30/38 | chr17 | 69086486 | |||||||
| chr17:69086486 | A | AATATATA others(17): Show |
3 | a0002c0002t0002g0027a0002c0002t0002g0182a0002c0002t0002g0219 | 4 | HG02165.hp1 NA18945.hp2 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.3937+108_3937+131d others(26): Show |
ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 30/38 | chr17 | 69086486 | |||||||
| chr17:69086486 | A | AATATATA others(21): Show |
1 | a0002c0002t0002g0009 | 3 | NA18612.hp2 NA19063.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.3937+131_3937+132i others(30): Show |
ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 30/38 | chr17 | 69086486 | |||||||
| chr17:69086486 | A | AATATATA others(23): Show |
1 | a0002c0002t0002g0201 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3937+131_3937+132i others(32): Show |
ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 30/38 | chr17 | 69086486 | |||||||
| chr17:69086486 | A | AATATATA others(25): Show |
1 | a0002c0002t0002g0214 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.3937+131_3937+132i others(34): Show |
ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 30/38 | chr17 | 69086486 | |||||||
| chr17:69086486 | A | AATATATA others(29): Show |
1 | a0002c0002t0002g0200 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3937+131_3937+132i others(38): Show |
ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 30/38 | chr17 | 69086486 | |||||||
| chr17:69086486 | A | AATATATA others(31): Show |
2 | a0002c0002t0002g0194a0002c0002t0002g0232 | 2 | HG02083.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.3937+131_3937+132i others(40): Show |
ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 30/38 | chr17 | 69086486 | |||||||
| chr17:69086486 | A | AATATATA others(39): Show |
3 | a0002c0002t0002g0170a0002c0002t0002g0233a0002c0002t0002g0234 | 3 | HG03139.hp2 NA18973.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.3937+131_3937+132i others(48): Show |
ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 30/38 | chr17 | 69086486 | |||||||
| chr17:69086486 | A | ATATATAT others(30): Show |
1 | a0002c0002t0002g0191 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.3937+131_3937+132i others(39): Show |
ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 30/38 | chr17 | 69086486 | |||||||
| chr17:69086486 | AAT | A | 14 | a0001c0001t0001g0065a0001c0001t0001g0071a0001c0001t0001g0073others(11): Show | 14 | HG00140.hp2 HG00639.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.3937+130_3937+131d others(4): Show |
ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 30/38 | chr17 | 69086486 | |||||||
| chr17:69086486 | AATAT | A | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(104): Show | 134 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.3937+128_3937+131d others(6): Show |
ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 30/38 | chr17 | 69086486 | |||||||
| chr17:69086486 | AATATAT | A | 12 | a0002c0002t0001g0224a0002c0002t0002g0225a0002c0002t0002g0236others(9): Show | 12 | HG01346.hp1 HG01928.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.3937+126_3937+131d others(8): Show |
ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 30/38 | chr17 | 69086486 | |||||||
| chr17:69086512 | G | T | 1 | a0003c0009t0001g0168 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3937+106C>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 30/38 | chr17 | 69086512 | |||||||
| chr17:69086567 | G | T | 1 | a0003c0003t0001g0273 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3937+51C>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 30/38 | chr17 | 69086567 | |||||||
| chr17:69086752 | C | A | 3 | a0002c0002t0002g0191a0002c0002t0002g0200a0002c0002t0002g0201 | 3 | HG02071.hp2 HG02074.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.3820-17G>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 29/38 | chr17 | 69086752 | |||||||
| chr17:69086821 | C | G | 69 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0026others(66): Show | 77 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.3820-86G>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 29/38 | chr17 | 69086821 | |||||||
| chr17:69086998 | A | C | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(142): Show | 177 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.3820-263T>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 29/38 | chr17 | 69086998 | |||||||
| chr17:69087018 | A | G | 1 | a0013c0016t0001g0159 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3820-283T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 29/38 | chr17 | 69087018 | |||||||
| chr17:69087187 | G | A | 1 | a0009c0012t0002g0139 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.3819+166C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 29/38 | chr17 | 69087187 | |||||||
| chr17:69087233 | G | A | 1 | a0006c0013t0001g0246 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3819+120C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 29/38 | chr17 | 69087233 | |||||||
| chr17:69087342 | T | C | 1 | a0002c0002t0002g0211 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.3819+11A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 29/38 | chr17 | 69087342 | |||||||
| chr17:69087600 | T | C | 2 | a0011c0011t0001g0043a0011c0011t0001g0044 | 2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3699-127A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 28/38 | chr17 | 69087600 | |||||||
| chr17:69087661 | A | G | 267 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(264): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.3699-188T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 28/38 | chr17 | 69087661 | |||||||
| chr17:69087912 | C | T | 2 | a0011c0011t0001g0043a0011c0011t0001g0044 | 2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3698+255G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 28/38 | chr17 | 69087912 | |||||||
| chr17:69087918 | C | T | 1 | a0015c0029t0001g0240 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3698+249G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 28/38 | chr17 | 69087918 | |||||||
| chr17:69088031 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3698+136G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 28/38 | chr17 | 69088031 | |||||||
| chr17:69088549 | T | A | 2 | a0003c0009t0001g0167a0003c0009t0001g0258 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.3607-291A>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 27/38 | chr17 | 69088549 | |||||||
| chr17:69088614 | T | C | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(202): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.3607-356A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 27/38 | chr17 | 69088614 | |||||||
| chr17:69088636 | C | G | 1 | a0001c0001t0001g0078 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.3607-378G>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 27/38 | chr17 | 69088636 | |||||||
| chr17:69088701 | T | C | 1 | a0002c0002t0002g0254 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.3607-443A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 27/38 | chr17 | 69088701 | |||||||
| chr17:69088858 | G | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0091 | 3 | NA18963.hp2 NA19001.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.3607-600C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 27/38 | chr17 | 69088858 | |||||||
| chr17:69088883 | G | A | 1 | a0003c0003t0001g0262 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3606+582C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 27/38 | chr17 | 69088883 | |||||||
| chr17:69088921 | C | T | 92 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0026others(89): Show | 100 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.3606+544G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 27/38 | chr17 | 69088921 | |||||||
| chr17:69089138 | T | A | 11 | a0003c0009t0001g0167a0003c0009t0001g0168a0003c0009t0001g0258others(8): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.3606+327A>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 27/38 | chr17 | 69089138 | |||||||
| chr17:69089180 | T | A | 1 | a0002c0002t0002g0238 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3606+285A>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 27/38 | chr17 | 69089180 | |||||||
| chr17:69089275 | T | C | 1 | a0004c0004t0002g0145 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.3606+190A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 27/38 | chr17 | 69089275 | |||||||
| chr17:69089316 | A | G | 31 | a0004c0004t0002g0006a0004c0004t0002g0021a0004c0004t0002g0022others(28): Show | 38 | HG00609.hp1 HG01074.hp1 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.3606+149T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 27/38 | chr17 | 69089316 | |||||||
| chr17:69089367 | A | G | 31 | a0004c0004t0002g0006a0004c0004t0002g0021a0004c0004t0002g0022others(28): Show | 38 | HG00609.hp1 HG01074.hp1 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.3606+98T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 27/38 | chr17 | 69089367 | |||||||
| chr17:69089444 | G | A | 3 | a0006c0010t0001g0255a0006c0010t0001g0256a0006c0010t0001g0257 | 3 | HG01884.hp1 HG03225.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3606+21C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 27/38 | chr17 | 69089444 | |||||||
| chr17:69089697 | G | A | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(94): Show | 118 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.3529-155C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 26/38 | chr17 | 69089697 | |||||||
| chr17:69089823 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3529-281C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 26/38 | chr17 | 69089823 | |||||||
| chr17:69089867 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3529-325A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 26/38 | chr17 | 69089867 | |||||||
| chr17:69089884 | G | A | 4 | a0001c0001t0001g0013a0001c0001t0001g0039a0001c0001t0001g0040others(1): Show | 5 | HG00323.hp2 HG00738.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.3529-342C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 26/38 | chr17 | 69089884 | |||||||
| chr17:69089993 | T | C | 96 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(93): Show | 117 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.3529-451A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 26/38 | chr17 | 69089993 | |||||||
| chr17:69090069 | A | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(189): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.3529-527T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 26/38 | chr17 | 69090069 | |||||||
| chr17:69090133 | G | T | 1 | a0002c0002t0002g0162 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.3529-591C>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 26/38 | chr17 | 69090133 | |||||||
| chr17:69090181 | T | A | 2 | a0001c0001t0001g0065a0001c0001t0001g0071 | 2 | HG01361.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.3529-639A>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 26/38 | chr17 | 69090181 | |||||||
| chr17:69090321 | C | T | 1 | a0015c0029t0001g0240 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3529-779G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 26/38 | chr17 | 69090321 | |||||||
| chr17:69090423 | T | C | 1 | a0015c0029t0001g0240 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3528+720A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 26/38 | chr17 | 69090423 | |||||||
| chr17:69090486 | G | A | 14 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0259others(11): Show | 18 | HG00639.hp2 HG01109.hp1 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.3528+657C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 26/38 | chr17 | 69090486 | |||||||
| chr17:69090512 | T | C | 1 | a0002c0002t0002g0223 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3528+631A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 26/38 | chr17 | 69090512 | |||||||
| chr17:69090583 | T | C | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(202): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.3528+560A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 26/38 | chr17 | 69090583 | |||||||
| chr17:69090764 | G | A | 2 | a0001c0001t0001g0036a0001c0001t0001g0077 | 2 | HG01123.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.3528+379C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 26/38 | chr17 | 69090764 | |||||||
| chr17:69091016 | C | A | 1 | a0013c0016t0001g0159 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3528+127G>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 26/38 | chr17 | 69091016 | |||||||
| chr17:69091079 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3528+64A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 26/38 | chr17 | 69091079 | |||||||
| chr17:69091510 | ACCAAATA others(304): Show |
A | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(141): Show | 176 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.3409-559_3409-249d others(2): Show |
ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 25/38 | chr17 | 69091510 | |||||||
| chr17:69091523 | C | CT | 6 | a0002c0002t0002g0175a0002c0002t0002g0187a0002c0002t0002g0191others(3): Show | 6 | HG02486.hp1 HG02886.hp2 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.3409-262dupA | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 25/38 | chr17 | 69091523 | |||||||
| chr17:69091523 | C | CTTTTTTT others(3): Show |
1 | a0013c0016t0001g0159 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3409-271_3409-262d others(12): Show |
ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 25/38 | chr17 | 69091523 | |||||||
| chr17:69091758 | G | A | 1 | a0002c0002t0002g0254 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.3409-496C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 25/38 | chr17 | 69091758 | |||||||
| chr17:69091957 | TA | T | 25 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0259others(22): Show | 33 | HG00639.hp2 HG01069.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.3409-696delT | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 25/38 | chr17 | 69091957 | |||||||
| chr17:69091983 | G | A | 1 | a0007c0006t0001g0087 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3409-721C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 25/38 | chr17 | 69091983 | |||||||
| chr17:69092082 | T | C | 1 | a0005c0005t0002g0152 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3409-820A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 25/38 | chr17 | 69092082 | |||||||
| chr17:69092171 | T | C | 2 | a0001c0001t0001g0038a0001c0001t0001g0095 | 2 | NA19063.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.3409-909A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 25/38 | chr17 | 69092171 | |||||||
| chr17:69092270 | G | T | 2 | a0001c0001t0001g0049a0001c0001t0001g0051 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.3409-1008C>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 25/38 | chr17 | 69092270 | |||||||
| chr17:69092393 | G | A | 11 | a0003c0009t0001g0167a0003c0009t0001g0168a0003c0009t0001g0258others(8): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.3409-1131C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 25/38 | chr17 | 69092393 | |||||||
| chr17:69092544 | G | A | 5 | a0006c0007t0001g0008a0006c0007t0001g0023a0006c0007t0001g0024others(2): Show | 9 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.3409-1282C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 25/38 | chr17 | 69092544 | |||||||
| chr17:69092801 | T | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(190): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.3409-1539A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 25/38 | chr17 | 69092801 | |||||||
| chr17:69092897 | C | T | 113 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(110): Show | 139 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.3409-1635G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 25/38 | chr17 | 69092897 | |||||||
| chr17:69093175 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3409-1913G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 25/38 | chr17 | 69093175 | |||||||
| chr17:69093375 | C | T | 2 | a0011c0011t0001g0043a0011c0011t0001g0044 | 2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3409-2113G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 25/38 | chr17 | 69093375 | |||||||
| chr17:69093576 | A | G | 1 | a0002c0002t0002g0241 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3409-2314T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 25/38 | chr17 | 69093576 | |||||||
| chr17:69093935 | T | C | 2 | a0005c0005t0001g0157a0005c0005t0001g0158 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3408+2305A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 25/38 | chr17 | 69093935 | |||||||
| chr17:69094056 | C | T | 2 | a0011c0011t0001g0043a0011c0011t0001g0044 | 2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3408+2184G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 25/38 | chr17 | 69094056 | |||||||
| chr17:69094059 | G | A | 143 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(140): Show | 175 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.3408+2181C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 25/38 | chr17 | 69094059 | |||||||
| chr17:69094156 | A | C | 1 | a0001c0001t0001g0122 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3408+2084T>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 25/38 | chr17 | 69094156 | |||||||
| chr17:69094255 | A | C | 13 | a0003c0009t0001g0167a0003c0009t0001g0168a0003c0009t0001g0258others(10): Show | 17 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.3408+1985T>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 25/38 | chr17 | 69094255 | |||||||
| chr17:69094296 | T | A | 1 | a0002c0002t0002g0234 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.3408+1944A>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 25/38 | chr17 | 69094296 | |||||||
| chr17:69094298 | T | C | 1 | a0005c0005t0001g0158 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3408+1942A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 25/38 | chr17 | 69094298 | |||||||
| chr17:69094431 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.3408+1809A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 25/38 | chr17 | 69094431 | |||||||
| chr17:69094557 | G | A | 1 | a0004c0004t0002g0130 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.3408+1683C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 25/38 | chr17 | 69094557 | |||||||
| chr17:69095021 | G | A | 5 | a0006c0007t0001g0008a0006c0007t0001g0023a0006c0007t0001g0024others(2): Show | 9 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.3408+1219C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 25/38 | chr17 | 69095021 | |||||||
| chr17:69095249 | T | C | 1 | a0015c0029t0001g0240 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3408+991A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 25/38 | chr17 | 69095249 | |||||||
| chr17:69095293 | G | A | 1 | a0002c0002t0002g0217 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.3408+947C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 25/38 | chr17 | 69095293 | |||||||
| chr17:69095396 | A | T | 2 | a0006c0013t0001g0163a0006c0013t0001g0246 | 2 | HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3408+844T>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 25/38 | chr17 | 69095396 | |||||||
| chr17:69095512 | T | C | 2 | a0006c0013t0001g0163a0006c0013t0001g0246 | 2 | HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3408+728A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 25/38 | chr17 | 69095512 | |||||||
| chr17:69095544 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.3408+696G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 25/38 | chr17 | 69095544 | |||||||
| chr17:69095627 | G | T | 1 | a0005c0005t0002g0155 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.3408+613C>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 25/38 | chr17 | 69095627 | |||||||
| chr17:69095679 | A | C | 1 | a0005c0005t0002g0154 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3408+561T>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 25/38 | chr17 | 69095679 | |||||||
| chr17:69096375 | A | G | 2 | a0006c0013t0001g0163a0006c0013t0001g0246 | 2 | HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3295-22T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 24/38 | chr17 | 69096375 | |||||||
| chr17:69096405 | G | C | 2 | a0006c0013t0001g0163a0006c0013t0001g0246 | 2 | HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3295-52C>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 24/38 | chr17 | 69096405 | |||||||
| chr17:69096521 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3294+107C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 24/38 | chr17 | 69096521 | |||||||
| chr17:69096522 | T | C | 3 | a0006c0010t0001g0255a0006c0010t0001g0256a0006c0010t0001g0257 | 3 | HG01884.hp1 HG03225.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3294+106A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 24/38 | chr17 | 69096522 | |||||||
| chr17:69096536 | T | C | 1 | a0002c0002t0002g0210 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.3294+92A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 24/38 | chr17 | 69096536 | |||||||
| chr17:69096931 | T | A | 1 | a0007c0006t0001g0105 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3121-130A>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 23/38 | chr17 | 69096931 | |||||||
| chr17:69096938 | T | C | 2 | a0006c0013t0001g0163a0006c0013t0001g0246 | 2 | HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3121-137A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 23/38 | chr17 | 69096938 | |||||||
| chr17:69097038 | C | A | 3 | a0005c0005t0002g0007a0005c0005t0002g0151a0005c0005t0002g0152 | 5 | HG02040.hp1 HG03704.hp1 NA18940.hp2 others(2): Show |
intron_variant | MODIFIER | c.3121-237G>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 23/38 | chr17 | 69097038 | |||||||
| chr17:69097039 | A | C | 3 | a0005c0005t0002g0007a0005c0005t0002g0151a0005c0005t0002g0152 | 5 | HG02040.hp1 HG03704.hp1 NA18940.hp2 others(2): Show |
intron_variant | MODIFIER | c.3121-238T>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 23/38 | chr17 | 69097039 | |||||||
| chr17:69097126 | C | T | 1 | a0004c0004t0002g0033 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3121-325G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 23/38 | chr17 | 69097126 | |||||||
| chr17:69097128 | C | T | 2 | a0006c0013t0001g0163a0006c0013t0001g0246 | 2 | HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3121-327G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 23/38 | chr17 | 69097128 | |||||||
| chr17:69097288 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.3121-487C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 23/38 | chr17 | 69097288 | |||||||
| chr17:69097315 | C | T | 1 | a0007c0006t0001g0061 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3121-514G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 23/38 | chr17 | 69097315 | |||||||
| chr17:69097390 | CA | C | 40 | a0001c0001t0001g0040a0001c0001t0001g0096a0002c0002t0002g0175others(37): Show | 46 | HG00323.hp2 HG00639.hp2 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.3120+529delT | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 23/38 | chr17 | 69097390 | |||||||
| chr17:69097390 | CAA | C | 11 | a0003c0009t0001g0167a0003c0009t0001g0168a0003c0009t0001g0258others(8): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.3120+528_3120+529d others(4): Show |
ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 23/38 | chr17 | 69097390 | |||||||
| chr17:69097429 | G | A | 3 | a0002c0002t0002g0241a0002c0002t0002g0242a0002c0002t0002g0243 | 3 | HG01884.hp2 HG02818.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.3120+491C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 23/38 | chr17 | 69097429 | |||||||
| chr17:69097532 | C | G | 1 | a0011c0011t0001g0043 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3120+388G>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 23/38 | chr17 | 69097532 | |||||||
| chr17:69097560 | T | C | 6 | a0003c0009t0001g0167a0003c0009t0001g0168a0003c0009t0001g0258others(3): Show | 6 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.3120+360A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 23/38 | chr17 | 69097560 | |||||||
| chr17:69097602 | T | C | 1 | a0002c0002t0002g0182 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.3120+318A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 23/38 | chr17 | 69097602 | |||||||
| chr17:69098278 | A | G | 3 | a0006c0010t0001g0255a0006c0010t0001g0256a0006c0010t0001g0257 | 3 | HG01884.hp1 HG03225.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3013-251T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 22/38 | chr17 | 69098278 | |||||||
| chr17:69098368 | T | C | 12 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(9): Show | 12 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(9): Show |
intron_variant | MODIFIER | c.3013-341A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 22/38 | chr17 | 69098368 | |||||||
| chr17:69098460 | T | C | 1 | a0001c0001t0001g0093 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.3013-433A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 22/38 | chr17 | 69098460 | |||||||
| chr17:69098604 | A | T | 1 | a0013c0016t0001g0159 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3013-577T>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 22/38 | chr17 | 69098604 | |||||||
| chr17:69098625 | C | CA | 18 | a0001c0001t0001g0016a0001c0001t0001g0034a0001c0001t0001g0040others(15): Show | 23 | HG00323.hp2 HG00639.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.3013-599dupT | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 22/38 | chr17 | 69098625 | |||||||
| chr17:69098625 | C | CAA | 104 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(101): Show | 124 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.3013-600_3013-599d others(4): Show |
ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 22/38 | chr17 | 69098625 | |||||||
| chr17:69098625 | C | CAAA | 81 | a0001c0001t0001g0014a0001c0001t0001g0039a0001c0001t0001g0050others(78): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.3013-601_3013-599d others(5): Show |
ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 22/38 | chr17 | 69098625 | |||||||
| chr17:69098842 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.3013-815G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 22/38 | chr17 | 69098842 | |||||||
| chr17:69098852 | C | T | 1 | a0013c0016t0001g0159 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3013-825G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 22/38 | chr17 | 69098852 | |||||||
| chr17:69099077 | G | A | 2 | a0002c0002t0001g0025a0002c0002t0001g0169 | 3 | HG02055.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3013-1050C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 22/38 | chr17 | 69099077 | |||||||
| chr17:69099153 | C | T | 2 | a0001c0001t0001g0065a0001c0001t0001g0071 | 2 | HG01361.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.3013-1126G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 22/38 | chr17 | 69099153 | |||||||
| chr17:69099202 | G | C | 1 | a0004c0004t0002g0141 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3013-1175C>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 22/38 | chr17 | 69099202 | |||||||
| chr17:69099220 | T | C | 1 | a0001c0001t0001g0040 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.3013-1193A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 22/38 | chr17 | 69099220 | |||||||
| chr17:69099459 | C | T | 1 | a0004c0004t0002g0149 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3012+1338G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 22/38 | chr17 | 69099459 | |||||||
| chr17:69099628 | C | T | 2 | a0007c0006t0002g0035a0016c0018t0002g0060 | 2 | HG02622.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3012+1169G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 22/38 | chr17 | 69099628 | |||||||
| chr17:69099713 | C | G | 1 | a0002c0002t0002g0232 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3012+1084G>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 22/38 | chr17 | 69099713 | |||||||
| chr17:69099764 | C | T | 1 | a0002c0002t0002g0193 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3012+1033G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 22/38 | chr17 | 69099764 | |||||||
| chr17:69099813 | A | G | 1 | a0003c0003t0001g0273 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3012+984T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 22/38 | chr17 | 69099813 | |||||||
| chr17:69099933 | T | C | 2 | a0002c0002t0002g0214a0012c0024t0002g0215 | 2 | HG00544.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.3012+864A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 22/38 | chr17 | 69099933 | |||||||
| chr17:69099938 | T | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(189): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.3012+859A>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 22/38 | chr17 | 69099938 | |||||||
| chr17:69099948 | T | TC | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(189): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.3012+848dupG | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 22/38 | chr17 | 69099948 | |||||||
| chr17:69099980 | G | C | 1 | a0011c0011t0001g0044 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3012+817C>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 22/38 | chr17 | 69099980 | |||||||
| chr17:69100012 | C | T | 92 | a0002c0002t0001g0025a0002c0002t0001g0169a0002c0002t0001g0224others(89): Show | 101 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.3012+785G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 22/38 | chr17 | 69100012 | |||||||
| chr17:69100051 | G | T | 1 | a0002c0002t0002g0232 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3012+746C>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 22/38 | chr17 | 69100051 | |||||||
| chr17:69100062 | G | A | 3 | a0005c0005t0002g0131a0005c0005t0002g0132a0005c0005t0002g0160 | 3 | HG02886.hp2 HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3012+735C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 22/38 | chr17 | 69100062 | |||||||
| chr17:69100343 | G | A | 1 | a0005c0005t0002g0131 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3012+454C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 22/38 | chr17 | 69100343 | |||||||
| chr17:69100352 | TAAA | T | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(189): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.3012+442_3012+444d others(5): Show |
ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 22/38 | chr17 | 69100352 | |||||||
| chr17:69100366 | G | A | 1 | a0002c0002t0002g0236 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.3012+431C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 22/38 | chr17 | 69100366 | |||||||
| chr17:69100436 | A | G | 1 | a0004c0004t0002g0143 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.3012+361T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 22/38 | chr17 | 69100436 | |||||||
| chr17:69100550 | C | T | 92 | a0002c0002t0001g0025a0002c0002t0001g0169a0002c0002t0001g0224others(89): Show | 101 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.3012+247G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 22/38 | chr17 | 69100550 | |||||||
| chr17:69100607 | G | A | 3 | a0008c0008t0002g0020a0008c0008t0002g0133a0008c0008t0002g0134 | 4 | NA18974.hp1 NA18985.hp2 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.3012+190C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 22/38 | chr17 | 69100607 | |||||||
| chr17:69100631 | GA | G | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(202): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.3012+165delT | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 22/38 | chr17 | 69100631 | |||||||
| chr17:69100782 | A | G | 1 | a0003c0009t0001g0167 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3012+15T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 22/38 | chr17 | 69100782 | |||||||
| chr17:69101051 | G | A | 2 | a0006c0013t0001g0163a0006c0013t0001g0246 | 2 | HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2875-117C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 21/38 | chr17 | 69101051 | |||||||
| chr17:69101071 | T | C | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(189): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.2875-137A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 21/38 | chr17 | 69101071 | |||||||
| chr17:69101134 | A | G | 2 | a0002c0002t0001g0025a0002c0002t0001g0169 | 3 | HG02055.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2875-200T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 21/38 | chr17 | 69101134 | |||||||
| chr17:69101224 | T | C | 5 | a0006c0007t0001g0008a0006c0007t0001g0023a0006c0007t0001g0024others(2): Show | 9 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.2875-290A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 21/38 | chr17 | 69101224 | |||||||
| chr17:69101457 | G | T | 1 | a0004c0004t0002g0135 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2875-523C>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 21/38 | chr17 | 69101457 | |||||||
| chr17:69101561 | A | C | 2 | a0002c0002t0002g0184a0002c0002t0002g0185 | 2 | NA19010.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.2875-627T>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 21/38 | chr17 | 69101561 | |||||||
| chr17:69101595 | C | CA | 15 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0094others(12): Show | 19 | HG01516.hp2 HG02135.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.2875-662dupT | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 21/38 | chr17 | 69101595 | |||||||
| chr17:69101595 | CA | C | 5 | a0001c0001t0001g0015a0001c0001t0001g0070a0002c0002t0002g0177others(2): Show | 6 | HG01169.hp1 HG01169.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.2875-662delT | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 21/38 | chr17 | 69101595 | |||||||
| chr17:69101874 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2875-940G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 21/38 | chr17 | 69101874 | |||||||
| chr17:69101875 | G | A | 1 | a0015c0029t0001g0240 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2875-941C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 21/38 | chr17 | 69101875 | |||||||
| chr17:69102086 | C | T | 1 | a0011c0011t0001g0044 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2874+749G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 21/38 | chr17 | 69102086 | |||||||
| chr17:69102116 | C | A | 1 | a0001c0001t0001g0078 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2874+719G>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 21/38 | chr17 | 69102116 | |||||||
| chr17:69102216 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2874+619G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 21/38 | chr17 | 69102216 | |||||||
| chr17:69102289 | A | G | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(202): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.2874+546T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 21/38 | chr17 | 69102289 | |||||||
| chr17:69102446 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2874+389A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 21/38 | chr17 | 69102446 | |||||||
| chr17:69102721 | C | G | 1 | a0002c0002t0002g0192 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2874+114G>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 21/38 | chr17 | 69102721 | |||||||
| chr17:69102834 | C | A | 1 | a0001c0001t0001g0040 | 1 | HG00323.hp2 | splice_donor_variant&intron_variant | HIGH | c.2874+1G>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 21/38 | chr17 | 69102834 | |||||||
| chr17:69102986 | A | T | 1 | a0001c0001t0001g0068 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2741-18T>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 20/38 | chr17 | 69102986 | |||||||
| chr17:69102988 | A | G | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(92): Show | 116 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.2741-20T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 20/38 | chr17 | 69102988 | |||||||
| chr17:69103024 | C | T | 3 | a0003c0009t0001g0167a0003c0009t0001g0168a0003c0009t0001g0258 | 3 | HG01891.hp2 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2741-56G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 20/38 | chr17 | 69103024 | |||||||
| chr17:69103067 | G | A | 3 | a0002c0002t0002g0229a0002c0002t0002g0230a0002c0002t0002g0231 | 3 | HG00140.hp2 HG00639.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.2741-99C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 20/38 | chr17 | 69103067 | |||||||
| chr17:69103128 | C | T | 1 | a0003c0009t0001g0168 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2741-160G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 20/38 | chr17 | 69103128 | |||||||
| chr17:69103503 | C | T | 8 | a0006c0007t0001g0008a0006c0007t0001g0023a0006c0007t0001g0024others(5): Show | 12 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.2741-535G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 20/38 | chr17 | 69103503 | |||||||
| chr17:69103517 | A | G | 95 | a0001c0001t0001g0179a0001c0001t0001g0180a0002c0002t0001g0224others(92): Show | 103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.2741-549T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 20/38 | chr17 | 69103517 | |||||||
| chr17:69103554 | G | A | 14 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0259others(11): Show | 18 | HG00639.hp2 HG01109.hp1 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.2741-586C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 20/38 | chr17 | 69103554 | |||||||
| chr17:69103817 | G | A | 236 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(233): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.2741-849C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 20/38 | chr17 | 69103817 | |||||||
| chr17:69103877 | G | C | 3 | a0003c0009t0001g0167a0003c0009t0001g0168a0003c0009t0001g0258 | 3 | HG01891.hp2 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2741-909C>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 20/38 | chr17 | 69103877 | |||||||
| chr17:69103911 | C | CTTTTTTT others(2): Show |
8 | a0002c0002t0002g0185a0003c0003t0001g0267a0003c0003t0001g0268others(5): Show | 8 | HG01891.hp1 HG01891.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.2741-952_2741-944d others(11): Show |
ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 20/38 | chr17 | 69103911 | |||||||
| chr17:69103911 | C | CTTTTTTT others(3): Show |
25 | a0001c0001t0001g0084a0001c0001t0001g0103a0002c0002t0002g0026others(22): Show | 30 | HG00639.hp2 HG01069.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.2741-953_2741-944d others(12): Show |
ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 20/38 | chr17 | 69103911 | |||||||
| chr17:69103911 | C | CTTTTTTT others(4): Show |
173 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(170): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.2741-954_2741-944d others(13): Show |
ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 20/38 | chr17 | 69103911 | |||||||
| chr17:69103911 | C | CTTTTTTT others(5): Show |
26 | a0001c0001t0001g0046a0001c0001t0001g0056a0001c0001t0001g0062others(23): Show | 30 | HG00140.hp2 HG00639.hp1 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.2741-955_2741-944d others(14): Show |
ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 20/38 | chr17 | 69103911 | |||||||
| chr17:69103911 | C | CTTTTTTT others(6): Show |
4 | a0002c0002t0002g0237a0006c0010t0001g0255a0006c0010t0001g0256others(1): Show | 4 | HG01884.hp1 HG01928.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2741-956_2741-944d others(15): Show |
ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 20/38 | chr17 | 69103911 | |||||||
| chr17:69103911 | CT | C | 4 | a0004c0004t0002g0146a0005c0005t0002g0007a0005c0005t0002g0151others(1): Show | 6 | HG01167.hp2 HG02040.hp1 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.2741-944delA | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 20/38 | chr17 | 69103911 | |||||||
| chr17:69103974 | C | T | 1 | a0002c0002t0001g0224 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2741-1006G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 20/38 | chr17 | 69103974 | |||||||
| chr17:69104167 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2741-1199G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 20/38 | chr17 | 69104167 | |||||||
| chr17:69104467 | C | T | 26 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0030others(23): Show | 32 | HG00639.hp2 HG01099.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.2740+995G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 20/38 | chr17 | 69104467 | |||||||
| chr17:69104565 | A | AT | 32 | a0004c0004t0002g0006a0004c0004t0002g0021a0004c0004t0002g0022others(29): Show | 39 | HG00609.hp1 HG01074.hp1 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.2740+896dupA | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 20/38 | chr17 | 69104565 | |||||||
| chr17:69104657 | A | G | 2 | a0001c0001t0001g0065a0001c0001t0001g0071 | 2 | HG01361.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.2740+805T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 20/38 | chr17 | 69104657 | |||||||
| chr17:69104662 | AAC | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(95): Show | 117 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.2740+798_2740+799d others(4): Show |
ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 20/38 | chr17 | 69104662 | |||||||
| chr17:69104663 | AC | A | 149 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0042others(146): Show | 170 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.2740+798delG | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 20/38 | chr17 | 69104663 | |||||||
| chr17:69104664 | C | A | 17 | a0002c0002t0001g0224a0002c0002t0002g0173a0002c0002t0002g0183others(14): Show | 21 | HG00544.hp2 HG01069.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.2740+798G>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 20/38 | chr17 | 69104664 | |||||||
| chr17:69104672 | C | A | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(188): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.2740+790G>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 20/38 | chr17 | 69104672 | |||||||
| chr17:69104692 | G | A | 5 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0097others(2): Show | 5 | HG02559.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2740+770C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 20/38 | chr17 | 69104692 | |||||||
| chr17:69104696 | G | A | 1 | a0002c0002t0002g0244 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2740+766C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 20/38 | chr17 | 69104696 | |||||||
| chr17:69104739 | G | A | 2 | a0001c0001t0001g0179a0001c0001t0001g0180 | 2 | HG00323.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.2740+723C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 20/38 | chr17 | 69104739 | |||||||
| chr17:69104764 | G | A | 1 | a0003c0003t0001g0278 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2740+698C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 20/38 | chr17 | 69104764 | |||||||
| chr17:69104814 | CA | C | 8 | a0006c0007t0001g0008a0006c0007t0001g0023a0006c0007t0001g0024others(5): Show | 12 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.2740+647delT | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 20/38 | chr17 | 69104814 | |||||||
| chr17:69104831 | T | G | 3 | a0006c0010t0001g0255a0006c0010t0001g0256a0006c0010t0001g0257 | 3 | HG01884.hp1 HG03225.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2740+631A>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 20/38 | chr17 | 69104831 | |||||||
| chr17:69104907 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.2740+555C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 20/38 | chr17 | 69104907 | |||||||
| chr17:69104928 | C | T | 3 | a0004c0004t0002g0147a0005c0005t0001g0157a0005c0005t0001g0158 | 3 | HG01891.hp1 HG01978.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2740+534G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 20/38 | chr17 | 69104928 | |||||||
| chr17:69105000 | C | T | 62 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0030others(59): Show | 75 | HG00609.hp1 HG00639.hp2 HG01074.hp1 others(72): Show |
intron_variant | MODIFIER | c.2740+462G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 20/38 | chr17 | 69105000 | |||||||
| chr17:69105179 | T | C | 1 | a0001c0001t0001g0041 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2740+283A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 20/38 | chr17 | 69105179 | |||||||
| chr17:69105384 | CT | C | 4 | a0002c0002t0002g0248a0010c0014t0002g0247a0010c0014t0002g0250others(1): Show | 4 | HG02040.hp2 NA19054.hp2 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.2740+77delA | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 20/38 | chr17 | 69105384 | |||||||
| chr17:69105386 | T | C | 22 | a0002c0002t0002g0010a0002c0002t0002g0026a0002c0002t0002g0172others(19): Show | 25 | HG01123.hp2 HG01934.hp1 HG02015.hp2 others(22): Show |
intron_variant | MODIFIER | c.2740+76A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 20/38 | chr17 | 69105386 | |||||||
| chr17:69105437 | A | C | 3 | a0006c0010t0001g0255a0006c0010t0001g0256a0006c0010t0001g0257 | 3 | HG01884.hp1 HG03225.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2740+25T>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 20/38 | chr17 | 69105437 | |||||||
| chr17:69105674 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2574-46A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 19/38 | chr17 | 69105674 | |||||||
| chr17:69105862 | C | T | 5 | a0006c0007t0001g0008a0006c0007t0001g0023a0006c0007t0001g0024others(2): Show | 9 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.2573+166G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 19/38 | chr17 | 69105862 | |||||||
| chr17:69106332 | C | A | 62 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0030others(59): Show | 75 | HG00609.hp1 HG00639.hp2 HG01074.hp1 others(72): Show |
intron_variant | MODIFIER | c.2390-121G>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 18/38 | chr17 | 69106332 | |||||||
| chr17:69106356 | A | G | 267 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(264): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.2390-145T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 18/38 | chr17 | 69106356 | |||||||
| chr17:69106593 | G | GA | 229 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(226): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.2390-383dupT | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 18/38 | chr17 | 69106593 | |||||||
| chr17:69106593 | G | GAA | 20 | a0001c0001t0001g0056a0001c0001t0001g0079a0001c0001t0001g0080others(17): Show | 24 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.2390-384_2390-383d others(4): Show |
ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 18/38 | chr17 | 69106593 | |||||||
| chr17:69106726 | G | T | 264 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(261): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.2390-515C>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 18/38 | chr17 | 69106726 | |||||||
| chr17:69106924 | A | C | 1 | a0001c0001t0001g0064 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2390-713T>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 18/38 | chr17 | 69106924 | |||||||
| chr17:69106969 | T | A | 1 | a0004c0004t0002g0033 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2389+727A>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 18/38 | chr17 | 69106969 | |||||||
| chr17:69106970 | A | T | 180 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(177): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.2389+726T>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 18/38 | chr17 | 69106970 | |||||||
| chr17:69107155 | C | G | 1 | a0002c0002t0003g0228 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2389+541G>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 18/38 | chr17 | 69107155 | |||||||
| chr17:69107370 | C | A | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(188): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.2389+326G>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 18/38 | chr17 | 69107370 | |||||||
| chr17:69107961 | G | A | 1 | a0002c0002t0002g0162 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.2273-149C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 17/38 | chr17 | 69107961 | |||||||
| chr17:69107968 | C | T | 3 | a0006c0010t0001g0255a0006c0010t0001g0256a0006c0010t0001g0257 | 3 | HG01884.hp1 HG03225.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2273-156G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 17/38 | chr17 | 69107968 | |||||||
| chr17:69108183 | T | C | 1 | a0002c0002t0002g0212 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2273-371A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 17/38 | chr17 | 69108183 | |||||||
| chr17:69108353 | C | G | 30 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0030others(27): Show | 36 | HG00639.hp2 HG01099.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.2273-541G>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 17/38 | chr17 | 69108353 | |||||||
| chr17:69108366 | G | T | 1 | a0005c0005t0002g0128 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2273-554C>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 17/38 | chr17 | 69108366 | |||||||
| chr17:69108407 | C | A | 3 | a0006c0013t0001g0163a0006c0013t0001g0246a0015c0029t0001g0240 | 3 | HG02145.hp2 HG02622.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2273-595G>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 17/38 | chr17 | 69108407 | |||||||
| chr17:69108521 | G | C | 3 | a0003c0009t0001g0167a0003c0009t0001g0168a0003c0009t0001g0258 | 3 | HG01891.hp2 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2273-709C>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 17/38 | chr17 | 69108521 | |||||||
| chr17:69108770 | G | A | 1 | a0015c0029t0001g0240 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2273-958C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 17/38 | chr17 | 69108770 | |||||||
| chr17:69108778 | C | A | 5 | a0006c0007t0001g0008a0006c0007t0001g0023a0006c0007t0001g0024others(2): Show | 9 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.2273-966G>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 17/38 | chr17 | 69108778 | |||||||
| chr17:69108806 | G | A | 1 | a0001c0001t0001g0036 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2273-994C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 17/38 | chr17 | 69108806 | |||||||
| chr17:69108881 | T | C | 1 | a0004c0004t0002g0150 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.2273-1069A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 17/38 | chr17 | 69108881 | |||||||
| chr17:69109088 | T | C | 2 | a0002c0002t0002g0026a0002c0002t0002g0173 | 3 | NA18955.hp2 NA18963.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.2273-1276A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 17/38 | chr17 | 69109088 | |||||||
| chr17:69109203 | A | ATGTTTAA others(13): Show |
72 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0030others(69): Show | 85 | HG00609.hp1 HG00639.hp2 HG00733.hp1 others(82): Show |
intron_variant | MODIFIER | c.2273-1411_2273-139 others(24): Show |
ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 17/38 | chr17 | 69109203 | |||||||
| chr17:69109363 | G | A | 46 | a0004c0004t0002g0006a0004c0004t0002g0021a0004c0004t0002g0022others(43): Show | 53 | HG00609.hp1 HG00733.hp1 HG01070.hp1 others(50): Show |
intron_variant | MODIFIER | c.2272+1438C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 17/38 | chr17 | 69109363 | |||||||
| chr17:69109441 | G | T | 11 | a0006c0007t0001g0008a0006c0007t0001g0023a0006c0007t0001g0024others(8): Show | 15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.2272+1360C>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 17/38 | chr17 | 69109441 | |||||||
| chr17:69109451 | G | A | 2 | a0005c0005t0001g0157a0005c0005t0001g0158 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2272+1350C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 17/38 | chr17 | 69109451 | |||||||
| chr17:69109682 | C | G | 2 | a0002c0002t0002g0226a0002c0002t0002g0238 | 2 | HG03654.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.2272+1119G>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 17/38 | chr17 | 69109682 | |||||||
| chr17:69109738 | A | T | 1 | a0001c0001t0001g0059 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.2272+1063T>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 17/38 | chr17 | 69109738 | |||||||
| chr17:69109941 | T | C | 1 | a0024c0023t0002g0188 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2272+860A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 17/38 | chr17 | 69109941 | |||||||
| chr17:69109973 | CT | C | 8 | a0004c0004t0002g0006a0004c0004t0002g0142a0004c0004t0002g0143others(5): Show | 10 | HG01074.hp1 HG01167.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.2272+827delA | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 17/38 | chr17 | 69109973 | |||||||
| chr17:69110085 | A | G | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(186): Show | 228 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.2272+716T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 17/38 | chr17 | 69110085 | |||||||
| chr17:69110134 | C | T | 1 | a0002c0002t0002g0244 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2272+667G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 17/38 | chr17 | 69110134 | |||||||
| chr17:69110138 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.2272+663G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 17/38 | chr17 | 69110138 | |||||||
| chr17:69110167 | G | A | 5 | a0006c0007t0001g0008a0006c0007t0001g0023a0006c0007t0001g0024others(2): Show | 9 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.2272+634C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 17/38 | chr17 | 69110167 | |||||||
| chr17:69110221 | G | A | 1 | a0007c0006t0001g0088 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2272+580C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 17/38 | chr17 | 69110221 | |||||||
| chr17:69110224 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2272+577C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 17/38 | chr17 | 69110224 | |||||||
| chr17:69110272 | A | C | 1 | a0001c0001t0001g0059 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.2272+529T>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 17/38 | chr17 | 69110272 | |||||||
| chr17:69110614 | C | T | 1 | a0002c0002t0002g0189 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2272+187G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 17/38 | chr17 | 69110614 | |||||||
| chr17:69110672 | T | C | 1 | a0002c0002t0002g0238 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2272+129A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 17/38 | chr17 | 69110672 | |||||||
| chr17:69110721 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2272+80A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 17/38 | chr17 | 69110721 | |||||||
| chr17:69111092 | CA | C | 3 | a0003c0009t0001g0167a0003c0009t0001g0168a0003c0009t0001g0258 | 3 | HG01891.hp2 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2133-153delT | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 16/38 | chr17 | 69111092 | |||||||
| chr17:69111422 | T | A | 4 | a0001c0001t0001g0014a0001c0001t0001g0049a0001c0001t0001g0050others(1): Show | 5 | HG00642.hp1 HG00738.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.2133-482A>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 16/38 | chr17 | 69111422 | |||||||
| chr17:69111490 | C | T | 3 | a0006c0010t0001g0255a0006c0010t0001g0256a0006c0010t0001g0257 | 3 | HG01884.hp1 HG03225.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2133-550G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 16/38 | chr17 | 69111490 | |||||||
| chr17:69111549 | C | T | 100 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(97): Show | 121 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.2133-609G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 16/38 | chr17 | 69111549 | |||||||
| chr17:69111770 | T | C | 1 | a0002c0002t0002g0213 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2132+413A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 16/38 | chr17 | 69111770 | |||||||
| chr17:69111780 | C | T | 5 | a0003c0003t0001g0012a0003c0003t0001g0267a0003c0003t0001g0268others(2): Show | 7 | HG02451.hp1 HG02572.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.2132+403G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 16/38 | chr17 | 69111780 | |||||||
| chr17:69111893 | T | C | 1 | a0018c0022t0001g0272 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2132+290A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 16/38 | chr17 | 69111893 | |||||||
| chr17:69111914 | G | T | 2 | a0002c0002t0001g0025a0002c0002t0001g0169 | 3 | HG02055.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2132+269C>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 16/38 | chr17 | 69111914 | |||||||
| chr17:69111987 | C | T | 1 | a0022c0026t0002g0106 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2132+196G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 16/38 | chr17 | 69111987 | |||||||
| chr17:69112005 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2132+178T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 16/38 | chr17 | 69112005 | |||||||
| chr17:69112402 | T | C | 4 | a0005c0005t0001g0157a0005c0005t0001g0158a0011c0011t0001g0043others(1): Show | 4 | HG01891.hp1 HG03098.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2042-129A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 15/38 | chr17 | 69112402 | |||||||
| chr17:69112436 | T | C | 85 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0030others(82): Show | 102 | HG00609.hp1 HG00639.hp2 HG00733.hp1 others(99): Show |
intron_variant | MODIFIER | c.2042-163A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 15/38 | chr17 | 69112436 | |||||||
| chr17:69112577 | C | T | 3 | a0002c0002t0002g0241a0002c0002t0002g0242a0002c0002t0002g0243 | 3 | HG01884.hp2 HG02818.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2042-304G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 15/38 | chr17 | 69112577 | |||||||
| chr17:69112724 | T | A | 2 | a0003c0009t0001g0167a0003c0009t0001g0258 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.2042-451A>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 15/38 | chr17 | 69112724 | |||||||
| chr17:69112741 | T | C | 85 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0030others(82): Show | 102 | HG00609.hp1 HG00639.hp2 HG00733.hp1 others(99): Show |
intron_variant | MODIFIER | c.2042-468A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 15/38 | chr17 | 69112741 | |||||||
| chr17:69112751 | C | T | 5 | a0003c0003t0001g0030a0003c0003t0001g0031a0003c0003t0001g0266others(2): Show | 7 | HG01099.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2041+471G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 15/38 | chr17 | 69112751 | |||||||
| chr17:69112874 | GA | G | 28 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0030others(25): Show | 34 | HG00639.hp2 HG01099.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.2041+347delT | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 15/38 | chr17 | 69112874 | |||||||
| chr17:69113150 | C | A | 1 | a0002c0002t0002g0222 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2041+72G>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 15/38 | chr17 | 69113150 | |||||||
| chr17:69113402 | A | T | 1 | a0002c0002t0002g0187 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1903-42T>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 14/38 | chr17 | 69113402 | |||||||
| chr17:69113521 | G | A | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(96): Show | 120 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.1902+97C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 14/38 | chr17 | 69113521 | |||||||
| chr17:69113532 | A | G | 82 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(79): Show | 103 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.1902+86T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 14/38 | chr17 | 69113532 | |||||||
| chr17:69113583 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1902+35C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 14/38 | chr17 | 69113583 | |||||||
| chr17:69113598 | C | G | 1 | a0001c0001t0001g0122 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1902+20G>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 14/38 | chr17 | 69113598 | |||||||
| chr17:69113753 | C | T | 101 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(98): Show | 122 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.1783-16G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 13/38 | chr17 | 69113753 | |||||||
| chr17:69113856 | A | G | 46 | a0004c0004t0002g0006a0004c0004t0002g0021a0004c0004t0002g0022others(43): Show | 53 | HG00609.hp1 HG00733.hp1 HG01070.hp1 others(50): Show |
intron_variant | MODIFIER | c.1783-119T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 13/38 | chr17 | 69113856 | |||||||
| chr17:69113875 | C | T | 1 | a0007c0006t0001g0061 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1783-138G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 13/38 | chr17 | 69113875 | |||||||
| chr17:69113891 | G | A | 9 | a0001c0001t0001g0013a0001c0001t0001g0039a0001c0001t0001g0040others(6): Show | 10 | HG00323.hp2 HG00738.hp1 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.1783-154C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 13/38 | chr17 | 69113891 | |||||||
| chr17:69113941 | T | G | 1 | a0001c0001t0001g0114 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1783-204A>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 13/38 | chr17 | 69113941 | |||||||
| chr17:69113949 | T | C | 31 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0030others(28): Show | 37 | HG00639.hp2 HG01099.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.1783-212A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 13/38 | chr17 | 69113949 | |||||||
| chr17:69114006 | C | T | 1 | a0006c0013t0001g0246 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1783-269G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 13/38 | chr17 | 69114006 | |||||||
| chr17:69114114 | C | T | 1 | a0003c0003t0001g0030 | 2 | HG01099.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1783-377G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 13/38 | chr17 | 69114114 | |||||||
| chr17:69114115 | G | A | 1 | a0006c0010t0001g0255 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1783-378C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 13/38 | chr17 | 69114115 | |||||||
| chr17:69114226 | T | C | 77 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0030others(74): Show | 90 | HG00609.hp1 HG00639.hp2 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.1783-489A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 13/38 | chr17 | 69114226 | |||||||
| chr17:69114441 | C | A | 1 | a0002c0002t0002g0170 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1782+321G>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 13/38 | chr17 | 69114441 | |||||||
| chr17:69114470 | C | T | 1 | a0002c0002t0001g0224 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1782+292G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 13/38 | chr17 | 69114470 | |||||||
| chr17:69114481 | G | C | 46 | a0004c0004t0002g0006a0004c0004t0002g0021a0004c0004t0002g0022others(43): Show | 53 | HG00609.hp1 HG00733.hp1 HG01070.hp1 others(50): Show |
intron_variant | MODIFIER | c.1782+281C>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 13/38 | chr17 | 69114481 | |||||||
| chr17:69114503 | A | G | 1 | a0002c0002t0002g0162 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1782+259T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 13/38 | chr17 | 69114503 | |||||||
| chr17:69114628 | G | A | 1 | a0003c0003t0001g0032 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1782+134C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 13/38 | chr17 | 69114628 | |||||||
| chr17:69115214 | A | T | 4 | a0002c0002t0002g0026a0002c0002t0002g0173a0002c0002t0002g0184others(1): Show | 5 | NA18955.hp2 NA18963.hp1 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.1606+162T>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 12/38 | chr17 | 69115214 | |||||||
| chr17:69115874 | T | G | 3 | a0006c0010t0001g0255a0006c0010t0001g0256a0006c0010t0001g0257 | 3 | HG01884.hp1 HG03225.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1496-388A>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 11/38 | chr17 | 69115874 | |||||||
| chr17:69116188 | G | A | 1 | a0005c0005t0001g0157 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1496-702C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 11/38 | chr17 | 69116188 | |||||||
| chr17:69116233 | T | C | 1 | a0002c0002t0002g0253 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1496-747A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 11/38 | chr17 | 69116233 | |||||||
| chr17:69116315 | C | G | 111 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(108): Show | 132 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.1496-829G>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 11/38 | chr17 | 69116315 | |||||||
| chr17:69116322 | A | G | 25 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0030others(22): Show | 31 | HG00639.hp2 HG01099.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.1496-836T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 11/38 | chr17 | 69116322 | |||||||
| chr17:69116873 | C | T | 2 | a0001c0001t0001g0002a0001c0001t0001g0111 | 5 | HG01943.hp2 HG01952.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.1495+1025G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 11/38 | chr17 | 69116873 | |||||||
| chr17:69117045 | TAAAG | T | 5 | a0006c0007t0001g0008a0006c0007t0001g0023a0006c0007t0001g0024others(2): Show | 9 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.1495+849_1495+852d others(6): Show |
ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 11/38 | chr17 | 69117045 | |||||||
| chr17:69117094 | A | G | 14 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0259others(11): Show | 18 | HG00639.hp2 HG01109.hp1 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.1495+804T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 11/38 | chr17 | 69117094 | |||||||
| chr17:69117144 | T | C | 2 | a0001c0001t0001g0097a0001c0001t0001g0098 | 2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1495+754A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 11/38 | chr17 | 69117144 | |||||||
| chr17:69117200 | C | T | 5 | a0005c0005t0002g0123a0005c0005t0002g0124a0005c0005t0002g0125others(2): Show | 5 | HG01070.hp1 HG01071.hp1 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.1495+698G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 11/38 | chr17 | 69117200 | |||||||
| chr17:69117221 | G | A | 25 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0030others(22): Show | 31 | HG00639.hp2 HG01099.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.1495+677C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 11/38 | chr17 | 69117221 | |||||||
| chr17:69117388 | TA | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0059 | 4 | NA18957.hp1 NA18969.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.1495+509delT | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 11/38 | chr17 | 69117388 | |||||||
| chr17:69117708 | G | T | 1 | a0011c0011t0001g0043 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1495+190C>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 11/38 | chr17 | 69117708 | |||||||
| chr17:69118009 | C | T | 1 | a0002c0002t0002g0225 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1437-53G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 10/38 | chr17 | 69118009 | |||||||
| chr17:69118345 | A | G | 3 | a0006c0007t0001g0023a0006c0007t0001g0024a0006c0007t0001g0165 | 5 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.1437-389T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 10/38 | chr17 | 69118345 | |||||||
| chr17:69118681 | C | T | 4 | a0001c0001t0001g0045a0001c0001t0001g0052a0001c0001t0001g0053others(1): Show | 4 | HG03704.hp2 HG03942.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.1437-725G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 10/38 | chr17 | 69118681 | |||||||
| chr17:69118796 | T | C | 1 | a0004c0004t0002g0130 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1437-840A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 10/38 | chr17 | 69118796 | |||||||
| chr17:69118934 | T | A | 1 | a0001c0001t0001g0038 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1437-978A>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 10/38 | chr17 | 69118934 | |||||||
| chr17:69118936 | A | T | 86 | a0002c0002t0002g0183a0003c0003t0001g0011a0003c0003t0001g0012others(83): Show | 103 | HG00609.hp1 HG00639.hp2 HG00733.hp1 others(100): Show |
intron_variant | MODIFIER | c.1437-980T>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 10/38 | chr17 | 69118936 | |||||||
| chr17:69119017 | A | G | 2 | a0007c0006t0002g0035a0016c0018t0002g0060 | 2 | HG02622.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1437-1061T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 10/38 | chr17 | 69119017 | |||||||
| chr17:69119617 | C | T | 46 | a0004c0004t0002g0006a0004c0004t0002g0021a0004c0004t0002g0022others(43): Show | 53 | HG00609.hp1 HG00733.hp1 HG01070.hp1 others(50): Show |
intron_variant | MODIFIER | c.1437-1661G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 10/38 | chr17 | 69119617 | |||||||
| chr17:69119624 | T | C | 76 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0030others(73): Show | 89 | HG00609.hp1 HG00639.hp2 HG00733.hp1 others(86): Show |
intron_variant | MODIFIER | c.1437-1668A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 10/38 | chr17 | 69119624 | |||||||
| chr17:69119642 | G | A | 2 | a0002c0002t0001g0025a0002c0002t0001g0169 | 3 | HG02055.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1437-1686C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 10/38 | chr17 | 69119642 | |||||||
| chr17:69119698 | T | C | 1 | a0007c0006t0002g0110 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1437-1742A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 10/38 | chr17 | 69119698 | |||||||
| chr17:69119706 | T | C | 10 | a0001c0001t0001g0018a0001c0001t0001g0038a0001c0001t0001g0058others(7): Show | 11 | HG00609.hp2 HG02135.hp1 NA18962.hp1 others(8): Show |
intron_variant | MODIFIER | c.1437-1750A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 10/38 | chr17 | 69119706 | |||||||
| chr17:69119741 | T | C | 85 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0030others(82): Show | 102 | HG00609.hp1 HG00639.hp2 HG00733.hp1 others(99): Show |
intron_variant | MODIFIER | c.1437-1785A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 10/38 | chr17 | 69119741 | |||||||
| chr17:69119866 | C | T | 2 | a0004c0004t0002g0021a0004c0004t0002g0135 | 3 | NA18945.hp1 NA18965.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1437-1910G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 10/38 | chr17 | 69119866 | |||||||
| chr17:69119909 | G | C | 1 | a0003c0009t0001g0167 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1437-1953C>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 10/38 | chr17 | 69119909 | |||||||
| chr17:69119962 | T | G | 1 | a0005c0005t0002g0132 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1437-2006A>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 10/38 | chr17 | 69119962 | |||||||
| chr17:69120178 | C | T | 1 | a0006c0010t0001g0257 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1437-2222G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 10/38 | chr17 | 69120178 | |||||||
| chr17:69120310 | C | T | 3 | a0006c0013t0001g0163a0006c0013t0001g0246a0015c0029t0001g0240 | 3 | HG02145.hp2 HG02622.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1437-2354G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 10/38 | chr17 | 69120310 | |||||||
| chr17:69120465 | G | A | 2 | a0003c0009t0001g0167a0003c0009t0001g0168 | 2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1437-2509C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 10/38 | chr17 | 69120465 | |||||||
| chr17:69120544 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1437-2588C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 10/38 | chr17 | 69120544 | |||||||
| chr17:69120744 | G | T | 1 | a0002c0002t0001g0224 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1436+2495C>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 10/38 | chr17 | 69120744 | |||||||
| chr17:69121069 | T | C | 1 | a0005c0005t0001g0158 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1436+2170A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 10/38 | chr17 | 69121069 | |||||||
| chr17:69121221 | T | G | 9 | a0003c0009t0001g0258a0006c0007t0001g0008a0006c0007t0001g0023others(6): Show | 13 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.1436+2018A>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 10/38 | chr17 | 69121221 | |||||||
| chr17:69121274 | C | A | 1 | a0001c0001t0001g0098 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1436+1965G>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 10/38 | chr17 | 69121274 | |||||||
| chr17:69121287 | A | G | 76 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0030others(73): Show | 89 | HG00609.hp1 HG00639.hp2 HG00733.hp1 others(86): Show |
intron_variant | MODIFIER | c.1436+1952T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 10/38 | chr17 | 69121287 | |||||||
| chr17:69121385 | A | G | 46 | a0004c0004t0002g0006a0004c0004t0002g0021a0004c0004t0002g0022others(43): Show | 53 | HG00609.hp1 HG00733.hp1 HG01070.hp1 others(50): Show |
intron_variant | MODIFIER | c.1436+1854T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 10/38 | chr17 | 69121385 | |||||||
| chr17:69121404 | G | T | 2 | a0003c0009t0001g0167a0003c0009t0001g0168 | 2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1436+1835C>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 10/38 | chr17 | 69121404 | |||||||
| chr17:69121547 | A | G | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(186): Show | 228 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.1436+1692T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 10/38 | chr17 | 69121547 | |||||||
| chr17:69121746 | T | A | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(183): Show | 224 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.1436+1493A>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 10/38 | chr17 | 69121746 | |||||||
| chr17:69122105 | G | A | 1 | a0002c0002t0002g0214 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1436+1134C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 10/38 | chr17 | 69122105 | |||||||
| chr17:69122381 | T | C | 190 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(187): Show | 229 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.1436+858A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 10/38 | chr17 | 69122381 | |||||||
| chr17:69122439 | T | C | 5 | a0006c0007t0001g0008a0006c0007t0001g0023a0006c0007t0001g0024others(2): Show | 9 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.1436+800A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 10/38 | chr17 | 69122439 | |||||||
| chr17:69122472 | C | T | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | HG01346.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1436+767G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 10/38 | chr17 | 69122472 | |||||||
| chr17:69122476 | G | A | 85 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0030others(82): Show | 102 | HG00609.hp1 HG00639.hp2 HG00733.hp1 others(99): Show |
intron_variant | MODIFIER | c.1436+763C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 10/38 | chr17 | 69122476 | |||||||
| chr17:69122493 | C | T | 2 | a0003c0003t0001g0267a0003c0003t0001g0268 | 2 | HG02451.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1436+746G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 10/38 | chr17 | 69122493 | |||||||
| chr17:69122613 | G | T | 4 | a0001c0001t0001g0014a0001c0001t0001g0049a0001c0001t0001g0050others(1): Show | 5 | HG00642.hp1 HG00738.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.1436+626C>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 10/38 | chr17 | 69122613 | |||||||
| chr17:69122646 | A | G | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(185): Show | 226 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1436+593T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 10/38 | chr17 | 69122646 | |||||||
| chr17:69122710 | G | C | 1 | a0012c0024t0002g0215 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1436+529C>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 10/38 | chr17 | 69122710 | |||||||
| chr17:69122822 | T | G | 1 | a0001c0001t0001g0121 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1436+417A>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 10/38 | chr17 | 69122822 | |||||||
| chr17:69122836 | C | T | 5 | a0006c0007t0001g0008a0006c0007t0001g0023a0006c0007t0001g0024others(2): Show | 9 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.1436+403G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 10/38 | chr17 | 69122836 | |||||||
| chr17:69122861 | C | A | 1 | a0001c0001t0001g0108 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1436+378G>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 10/38 | chr17 | 69122861 | |||||||
| chr17:69123032 | A | G | 1 | a0001c0001t0001g0059 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1436+207T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 10/38 | chr17 | 69123032 | |||||||
| chr17:69123422 | G | C | 2 | a0001c0001t0001g0097a0001c0001t0001g0098 | 2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1268-15C>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 9/38 | chr17 | 69123422 | |||||||
| chr17:69123452 | G | C | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(145): Show | 176 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.1268-45C>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 9/38 | chr17 | 69123452 | |||||||
| chr17:69123457 | C | T | 1 | a0002c0002t0002g0172 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1268-50G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 9/38 | chr17 | 69123457 | |||||||
| chr17:69123501 | T | G | 1 | a0006c0013t0001g0163 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1268-94A>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 9/38 | chr17 | 69123501 | |||||||
| chr17:69123539 | T | A | 1 | a0008c0008t0002g0134 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1268-132A>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 9/38 | chr17 | 69123539 | |||||||
| chr17:69123584 | T | C | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(145): Show | 176 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.1268-177A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 9/38 | chr17 | 69123584 | |||||||
| chr17:69123605 | C | A | 1 | a0004c0004t0002g0148 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1268-198G>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 9/38 | chr17 | 69123605 | |||||||
| chr17:69123767 | G | C | 1 | a0002c0002t0002g0245 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1268-360C>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 9/38 | chr17 | 69123767 | |||||||
| chr17:69123827 | T | C | 2 | a0005c0005t0002g0007a0005c0005t0002g0151 | 4 | HG02040.hp1 NA18940.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.1268-420A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 9/38 | chr17 | 69123827 | |||||||
| chr17:69123884 | A | G | 147 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(144): Show | 175 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1268-477T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 9/38 | chr17 | 69123884 | |||||||
| chr17:69123922 | T | A | 3 | a0006c0010t0001g0255a0006c0010t0001g0256a0006c0010t0001g0257 | 3 | HG01884.hp1 HG03225.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1268-515A>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 9/38 | chr17 | 69123922 | |||||||
| chr17:69124105 | T | C | 2 | a0002c0002t0002g0170a0002c0002t0002g0216 | 2 | NA18993.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1268-698A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 9/38 | chr17 | 69124105 | |||||||
| chr17:69124175 | A | C | 4 | a0003c0009t0001g0258a0006c0010t0001g0255a0006c0010t0001g0256others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1267+713T>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 9/38 | chr17 | 69124175 | |||||||
| chr17:69124292 | C | G | 1 | a0003c0003t0001g0259 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1267+596G>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 9/38 | chr17 | 69124292 | |||||||
| chr17:69124293 | A | T | 1 | a0003c0003t0001g0266 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1267+595T>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 9/38 | chr17 | 69124293 | |||||||
| chr17:69124416 | C | T | 1 | a0001c0001t0001g0058 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1267+472G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 9/38 | chr17 | 69124416 | |||||||
| chr17:69124440 | G | T | 1 | a0002c0002t0002g0182 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1267+448C>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 9/38 | chr17 | 69124440 | |||||||
| chr17:69124445 | A | G | 1 | a0007c0006t0002g0057 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1267+443T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 9/38 | chr17 | 69124445 | |||||||
| chr17:69124654 | T | G | 1 | a0002c0002t0001g0224 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1267+234A>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 9/38 | chr17 | 69124654 | |||||||
| chr17:69125120 | T | C | 1 | a0007c0006t0002g0099 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1120-85A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 8/38 | chr17 | 69125120 | |||||||
| chr17:69125169 | G | A | 1 | a0001c0001t0001g0119 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1120-134C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 8/38 | chr17 | 69125169 | |||||||
| chr17:69125392 | A | G | 1 | a0001c0001t0001g0056 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1120-357T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 8/38 | chr17 | 69125392 | |||||||
| chr17:69125404 | C | A | 1 | a0004c0004t0002g0153 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1120-369G>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 8/38 | chr17 | 69125404 | |||||||
| chr17:69125702 | C | A | 4 | a0003c0009t0001g0258a0006c0010t0001g0255a0006c0010t0001g0256others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1120-667G>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 8/38 | chr17 | 69125702 | |||||||
| chr17:69125798 | A | G | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(145): Show | 176 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.1120-763T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 8/38 | chr17 | 69125798 | |||||||
| chr17:69125891 | A | C | 1 | a0006c0031t0001g0252 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1120-856T>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 8/38 | chr17 | 69125891 | |||||||
| chr17:69125992 | A | G | 3 | a0005c0005t0002g0131a0005c0005t0002g0132a0005c0005t0002g0160 | 3 | HG02886.hp2 HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1120-957T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 8/38 | chr17 | 69125992 | |||||||
| chr17:69126006 | T | C | 1 | a0003c0003t0001g0264 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1120-971A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 8/38 | chr17 | 69126006 | |||||||
| chr17:69126024 | A | G | 1 | a0005c0005t0002g0154 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1120-989T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 8/38 | chr17 | 69126024 | |||||||
| chr17:69126042 | C | T | 2 | a0005c0005t0002g0124a0005c0005t0002g0125 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1120-1007G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 8/38 | chr17 | 69126042 | |||||||
| chr17:69126075 | A | G | 2 | a0001c0001t0001g0054a0001c0001t0001g0055 | 2 | HG01099.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1120-1040T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 8/38 | chr17 | 69126075 | |||||||
| chr17:69126088 | T | C | 1 | a0005c0005t0001g0157 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1120-1053A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 8/38 | chr17 | 69126088 | |||||||
| chr17:69126400 | C | T | 2 | a0002c0002t0001g0025a0002c0002t0001g0169 | 3 | HG02055.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1120-1365G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 8/38 | chr17 | 69126400 | |||||||
| chr17:69126425 | C | T | 5 | a0006c0007t0001g0008a0006c0007t0001g0023a0006c0007t0001g0024others(2): Show | 9 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.1120-1390G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 8/38 | chr17 | 69126425 | |||||||
| chr17:69126462 | T | C | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(155): Show | 190 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.1120-1427A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 8/38 | chr17 | 69126462 | |||||||
| chr17:69126492 | T | C | 1 | a0013c0016t0001g0159 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1120-1457A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 8/38 | chr17 | 69126492 | |||||||
| chr17:69126553 | C | T | 3 | a0005c0005t0001g0157a0005c0005t0001g0158a0006c0013t0001g0246 | 3 | HG01891.hp1 HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1120-1518G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 8/38 | chr17 | 69126553 | |||||||
| chr17:69126853 | A | G | 1 | a0006c0013t0001g0163 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1119+1766T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 8/38 | chr17 | 69126853 | |||||||
| chr17:69127019 | C | T | 190 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(187): Show | 229 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.1119+1600G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 8/38 | chr17 | 69127019 | |||||||
| chr17:69127169 | T | G | 13 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(10): Show | 13 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1119+1450A>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 8/38 | chr17 | 69127169 | |||||||
| chr17:69127482 | A | C | 5 | a0006c0007t0001g0008a0006c0007t0001g0023a0006c0007t0001g0024others(2): Show | 9 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.1119+1137T>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 8/38 | chr17 | 69127482 | |||||||
| chr17:69127649 | G | A | 4 | a0005c0005t0001g0157a0005c0005t0001g0158a0011c0011t0001g0043others(1): Show | 4 | HG01891.hp1 HG03098.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1119+970C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 8/38 | chr17 | 69127649 | |||||||
| chr17:69127770 | T | C | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(188): Show | 230 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.1119+849A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 8/38 | chr17 | 69127770 | |||||||
| chr17:69127774 | C | T | 4 | a0005c0005t0001g0157a0005c0005t0001g0158a0011c0011t0001g0043others(1): Show | 4 | HG01891.hp1 HG03098.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1119+845G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 8/38 | chr17 | 69127774 | |||||||
| chr17:69127853 | C | G | 1 | a0004c0004t0002g0130 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1119+766G>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 8/38 | chr17 | 69127853 | |||||||
| chr17:69127864 | A | C | 2 | a0003c0009t0001g0167a0003c0009t0001g0168 | 2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1119+755T>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 8/38 | chr17 | 69127864 | |||||||
| chr17:69127950 | C | G | 1 | a0006c0031t0001g0252 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1119+669G>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 8/38 | chr17 | 69127950 | |||||||
| chr17:69127997 | C | A | 2 | a0011c0011t0001g0043a0011c0011t0001g0044 | 2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1119+622G>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 8/38 | chr17 | 69127997 | |||||||
| chr17:69128161 | G | C | 4 | a0003c0009t0001g0258a0006c0010t0001g0255a0006c0010t0001g0256others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1119+458C>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 8/38 | chr17 | 69128161 | |||||||
| chr17:69128323 | T | C | 1 | a0002c0002t0002g0218 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1119+296A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 8/38 | chr17 | 69128323 | |||||||
| chr17:69128339 | G | C | 1 | a0002c0002t0002g0219 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1119+280C>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 8/38 | chr17 | 69128339 | |||||||
| chr17:69128471 | T | C | 1 | a0006c0010t0001g0256 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1119+148A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 8/38 | chr17 | 69128471 | |||||||
| chr17:69128560 | G | A | 4 | a0003c0009t0001g0258a0006c0010t0001g0255a0006c0010t0001g0256others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1119+59C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 8/38 | chr17 | 69128560 | |||||||
| chr17:69128599 | C | T | 1 | a0002c0002t0002g0181 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1119+20G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 8/38 | chr17 | 69128599 | |||||||
| chr17:69128612 | C | A | 3 | a0005c0005t0002g0124a0005c0005t0002g0125a0017c0030t0002g0129 | 3 | HG01070.hp1 HG01071.hp1 HG02895.hp2 |
splice_region_variant&intron_variant | LOW | c.1119+7G>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 8/38 | chr17 | 69128612 | |||||||
| chr17:69128864 | T | C | 4 | a0003c0009t0001g0258a0006c0010t0001g0255a0006c0010t0001g0256others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.934-60A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 7/38 | chr17 | 69128864 | |||||||
| chr17:69129000 | C | G | 1 | a0013c0016t0001g0159 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.934-196G>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 7/38 | chr17 | 69129000 | |||||||
| chr17:69129082 | G | T | 2 | a0001c0001t0001g0052a0001c0001t0001g0053 | 2 | HG03704.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.934-278C>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 7/38 | chr17 | 69129082 | |||||||
| chr17:69129196 | C | T | 10 | a0005c0005t0002g0123a0005c0005t0002g0124a0005c0005t0002g0125others(7): Show | 10 | HG00733.hp1 HG01070.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.934-392G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 7/38 | chr17 | 69129196 | |||||||
| chr17:69129197 | G | A | 1 | a0013c0016t0001g0159 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.934-393C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 7/38 | chr17 | 69129197 | |||||||
| chr17:69129236 | G | A | 4 | a0003c0009t0001g0258a0006c0010t0001g0255a0006c0010t0001g0256others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.933+374C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 7/38 | chr17 | 69129236 | |||||||
| chr17:69129868 | A | G | 1 | a0002c0002t0002g0178 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.792-117T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 6/38 | chr17 | 69129868 | |||||||
| chr17:69129908 | C | T | 1 | a0005c0005t0002g0128 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.792-157G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 6/38 | chr17 | 69129908 | |||||||
| chr17:69129966 | A | G | 1 | a0006c0013t0001g0246 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.792-215T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 6/38 | chr17 | 69129966 | |||||||
| chr17:69130144 | G | A | 2 | a0007c0006t0001g0104a0007c0006t0001g0105 | 2 | HG02723.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.792-393C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 6/38 | chr17 | 69130144 | |||||||
| chr17:69130221 | G | A | 5 | a0006c0007t0001g0008a0006c0007t0001g0023a0006c0007t0001g0024others(2): Show | 9 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.792-470C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 6/38 | chr17 | 69130221 | |||||||
| chr17:69130316 | CA | C | 8 | a0001c0001t0001g0014a0001c0001t0001g0049a0001c0001t0001g0050others(5): Show | 10 | HG00642.hp1 HG00738.hp2 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.792-566delT | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 6/38 | chr17 | 69130316 | |||||||
| chr17:69130393 | C | T | 1 | a0005c0005t0002g0123 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.792-642G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 6/38 | chr17 | 69130393 | |||||||
| chr17:69130423 | T | C | 146 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(143): Show | 174 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.792-672A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 6/38 | chr17 | 69130423 | |||||||
| chr17:69130767 | A | G | 25 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0030others(22): Show | 31 | HG00639.hp2 HG01099.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.792-1016T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 6/38 | chr17 | 69130767 | |||||||
| chr17:69130886 | A | C | 1 | a0003c0009t0001g0167 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.792-1135T>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 6/38 | chr17 | 69130886 | |||||||
| chr17:69131007 | A | T | 1 | a0005c0005t0001g0157 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.792-1256T>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 6/38 | chr17 | 69131007 | |||||||
| chr17:69131032 | A | G | 146 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(143): Show | 174 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.792-1281T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 6/38 | chr17 | 69131032 | |||||||
| chr17:69131131 | G | A | 1 | a0004c0004t0002g0149 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.792-1380C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 6/38 | chr17 | 69131131 | |||||||
| chr17:69131569 | T | C | 1 | a0002c0002t0002g0239 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.792-1818A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 6/38 | chr17 | 69131569 | |||||||
| chr17:69131573 | TA | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 187 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.792-1823delT | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 6/38 | chr17 | 69131573 | |||||||
| chr17:69131623 | A | C | 5 | a0006c0007t0001g0008a0006c0007t0001g0023a0006c0007t0001g0024others(2): Show | 9 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.792-1872T>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 6/38 | chr17 | 69131623 | |||||||
| chr17:69131781 | A | G | 41 | a0004c0004t0002g0006a0004c0004t0002g0021a0004c0004t0002g0022others(38): Show | 48 | HG00609.hp1 HG00733.hp1 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.791+1860T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 6/38 | chr17 | 69131781 | |||||||
| chr17:69131790 | T | C | 1 | a0001c0001t0001g0120 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.791+1851A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 6/38 | chr17 | 69131790 | |||||||
| chr17:69131936 | G | A | 1 | a0006c0031t0001g0252 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.791+1705C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 6/38 | chr17 | 69131936 | |||||||
| chr17:69132023 | T | G | 1 | a0002c0002t0002g0220 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.791+1618A>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 6/38 | chr17 | 69132023 | |||||||
| chr17:69132045 | C | T | 2 | a0005c0005t0002g0124a0005c0005t0002g0125 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.791+1596G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 6/38 | chr17 | 69132045 | |||||||
| chr17:69132149 | T | C | 1 | a0006c0010t0001g0257 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.791+1492A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 6/38 | chr17 | 69132149 | |||||||
| chr17:69132518 | T | A | 4 | a0005c0005t0001g0157a0005c0005t0001g0158a0011c0011t0001g0043others(1): Show | 4 | HG01891.hp1 HG03098.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.791+1123A>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 6/38 | chr17 | 69132518 | |||||||
| chr17:69132519 | C | A | 4 | a0005c0005t0001g0157a0005c0005t0001g0158a0011c0011t0001g0043others(1): Show | 4 | HG01891.hp1 HG03098.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.791+1122G>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 6/38 | chr17 | 69132519 | |||||||
| chr17:69132543 | C | T | 2 | a0011c0011t0001g0043a0011c0011t0001g0044 | 2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.791+1098G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 6/38 | chr17 | 69132543 | |||||||
| chr17:69132726 | C | T | 1 | a0006c0007t0001g0164 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.791+915G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 6/38 | chr17 | 69132726 | |||||||
| chr17:69132873 | A | AGT | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(156): Show | 191 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.791+766_791+767dup others(2): Show |
ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 6/38 | chr17 | 69132873 | |||||||
| chr17:69132898 | A | G | 9 | a0003c0009t0001g0258a0006c0007t0001g0008a0006c0007t0001g0023others(6): Show | 13 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.791+743T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 6/38 | chr17 | 69132898 | |||||||
| chr17:69132931 | TATGTA | T | 9 | a0005c0005t0002g0123a0005c0005t0002g0124a0005c0005t0002g0125others(6): Show | 9 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.791+705_791+709del others(5): Show |
ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 6/38 | chr17 | 69132931 | |||||||
| chr17:69132958 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.791+683A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 6/38 | chr17 | 69132958 | |||||||
| chr17:69132988 | G | T | 181 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(178): Show | 219 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.791+653C>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 6/38 | chr17 | 69132988 | |||||||
| chr17:69133022 | G | A | 2 | a0002c0002t0002g0175a0002c0002t0002g0221 | 2 | NA18940.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.791+619C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 6/38 | chr17 | 69133022 | |||||||
| chr17:69133053 | C | A | 1 | a0001c0001t0001g0107 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.791+588G>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 6/38 | chr17 | 69133053 | |||||||
| chr17:69133229 | A | T | 4 | a0003c0009t0001g0258a0006c0010t0001g0255a0006c0010t0001g0256others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.791+412T>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 6/38 | chr17 | 69133229 | |||||||
| chr17:69133255 | C | T | 1 | a0003c0003t0001g0032 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.791+386G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 6/38 | chr17 | 69133255 | |||||||
| chr17:69133291 | T | C | 3 | a0001c0001t0001g0005a0001c0001t0001g0042a0001c0001t0001g0108 | 5 | NA18952.hp2 NA18987.hp1 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.791+350A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 6/38 | chr17 | 69133291 | |||||||
| chr17:69133295 | G | A | 1 | a0006c0031t0001g0252 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.791+346C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 6/38 | chr17 | 69133295 | |||||||
| chr17:69133306 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.791+335A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 6/38 | chr17 | 69133306 | |||||||
| chr17:69133404 | A | C | 24 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0030others(21): Show | 30 | HG00639.hp2 HG01099.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.791+237T>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 6/38 | chr17 | 69133404 | |||||||
| chr17:69133422 | T | A | 1 | a0007c0006t0002g0110 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.791+219A>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 6/38 | chr17 | 69133422 | |||||||
| chr17:69133535 | G | A | 1 | a0003c0003t0001g0273 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.791+106C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 6/38 | chr17 | 69133535 | |||||||
| chr17:69133956 | G | A | 1 | a0002c0002t0002g0222 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.565-89C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 5/38 | chr17 | 69133956 | |||||||
| chr17:69134001 | C | T | 1 | a0006c0007t0001g0164 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.565-134G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 5/38 | chr17 | 69134001 | |||||||
| chr17:69134094 | T | A | 2 | a0011c0011t0001g0043a0011c0011t0001g0044 | 2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.565-227A>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 5/38 | chr17 | 69134094 | |||||||
| chr17:69134208 | C | T | 1 | a0015c0029t0001g0240 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.565-341G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 5/38 | chr17 | 69134208 | |||||||
| chr17:69134294 | G | A | 1 | a0003c0003t0001g0265 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.564+345C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 5/38 | chr17 | 69134294 | |||||||
| chr17:69134370 | T | A | 1 | a0005c0005t0002g0128 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.564+269A>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 5/38 | chr17 | 69134370 | |||||||
| chr17:69134790 | T | C | 1 | a0005c0005t0001g0157 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.461-48A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 4/38 | chr17 | 69134790 | |||||||
| chr17:69134888 | C | CTTTTTTT others(2): Show |
8 | a0003c0009t0001g0258a0006c0007t0001g0008a0006c0007t0001g0023others(5): Show | 12 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.461-155_461-147dup others(9): Show |
ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 4/38 | chr17 | 69134888 | |||||||
| chr17:69134888 | C | CTTTTTTT others(3): Show |
19 | a0001c0001t0001g0111a0003c0003t0001g0012a0003c0003t0001g0030others(16): Show | 23 | HG01099.hp2 HG01943.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.461-156_461-147dup others(10): Show |
ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 4/38 | chr17 | 69134888 | |||||||
| chr17:69134888 | C | CTTTTTTT others(4): Show |
154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.461-157_461-147dup others(11): Show |
ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 4/38 | chr17 | 69134888 | |||||||
| chr17:69134888 | C | CTTTTTTT others(5): Show |
78 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0114others(75): Show | 86 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.461-147_461-146ins others(12): Show |
ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 4/38 | chr17 | 69134888 | |||||||
| chr17:69134888 | C | CTTTTTTT others(6): Show |
3 | a0002c0002t0002g0173a0002c0002t0002g0174a0002c0002t0002g0175 | 3 | NA18940.hp1 NA19078.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.461-147_461-146ins others(13): Show |
ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 4/38 | chr17 | 69134888 | |||||||
| chr17:69134988 | T | C | 2 | a0011c0011t0001g0043a0011c0011t0001g0044 | 2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.461-246A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 4/38 | chr17 | 69134988 | |||||||
| chr17:69135124 | G | A | 2 | a0005c0005t0002g0007a0005c0005t0002g0151 | 4 | HG02040.hp1 NA18940.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.461-382C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 4/38 | chr17 | 69135124 | |||||||
| chr17:69135380 | C | T | 3 | a0005c0005t0001g0157a0011c0011t0001g0043a0011c0011t0001g0044 | 3 | HG03098.hp1 HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.461-638G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 4/38 | chr17 | 69135380 | |||||||
| chr17:69135418 | G | A | 1 | a0003c0003t0001g0274 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.460+674C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 4/38 | chr17 | 69135418 | |||||||
| chr17:69135513 | T | G | 5 | a0006c0007t0001g0008a0006c0007t0001g0023a0006c0007t0001g0024others(2): Show | 9 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.460+579A>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 4/38 | chr17 | 69135513 | |||||||
| chr17:69135757 | C | T | 3 | a0006c0010t0001g0255a0006c0010t0001g0256a0006c0010t0001g0257 | 3 | HG01884.hp1 HG03225.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.460+335G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 4/38 | chr17 | 69135757 | |||||||
| chr17:69135859 | T | C | 1 | a0005c0005t0002g0152 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.460+233A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 4/38 | chr17 | 69135859 | |||||||
| chr17:69135881 | T | C | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(183): Show | 224 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.460+211A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 4/38 | chr17 | 69135881 | |||||||
| chr17:69135914 | T | G | 2 | a0006c0013t0001g0163a0015c0029t0001g0240 | 2 | HG02622.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.460+178A>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 4/38 | chr17 | 69135914 | |||||||
| chr17:69136364 | T | C | 1 | a0004c0004t0002g0153 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.302-114A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 3/38 | chr17 | 69136364 | |||||||
| chr17:69136558 | T | G | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(183): Show | 224 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.302-308A>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 3/38 | chr17 | 69136558 | |||||||
| chr17:69136743 | A | G | 1 | a0002c0002t0002g0172 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.302-493T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 3/38 | chr17 | 69136743 | |||||||
| chr17:69136880 | G | A | 147 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(144): Show | 175 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.301+416C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 3/38 | chr17 | 69136880 | |||||||
| chr17:69137027 | A | G | 1 | a0001c0001t0001g0042 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.301+269T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 3/38 | chr17 | 69137027 | |||||||
| chr17:69137074 | A | G | 4 | a0001c0001t0001g0013a0001c0001t0001g0039a0001c0001t0001g0040others(1): Show | 5 | HG00323.hp2 HG00738.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.301+222T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 3/38 | chr17 | 69137074 | |||||||
| chr17:69137126 | A | C | 1 | a0002c0002t0002g0171 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.301+170T>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 3/38 | chr17 | 69137126 | |||||||
| chr17:69137211 | T | G | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(183): Show | 224 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.301+85A>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 3/38 | chr17 | 69137211 | |||||||
| chr17:69137279 | G | A | 6 | a0002c0002t0002g0241a0002c0002t0002g0242a0002c0002t0002g0243others(3): Show | 6 | HG01884.hp2 HG02523.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.301+17C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 3/38 | chr17 | 69137279 | |||||||
| chr17:69137541 | C | G | 1 | a0001c0001t0001g0038 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.97-41G>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 2/38 | chr17 | 69137541 | |||||||
| chr17:69137744 | G | A | 2 | a0001c0001t0001g0112a0001c0001t0001g0113 | 2 | NA19007.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.97-244C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 2/38 | chr17 | 69137744 | |||||||
| chr17:69137807 | T | C | 31 | a0004c0004t0002g0006a0004c0004t0002g0021a0004c0004t0002g0022others(28): Show | 38 | HG00609.hp1 HG01074.hp1 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.97-307A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 2/38 | chr17 | 69137807 | |||||||
| chr17:69137890 | T | C | 1 | a0006c0013t0001g0246 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.97-390A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 2/38 | chr17 | 69137890 | |||||||
| chr17:69138039 | C | A | 5 | a0006c0007t0001g0008a0006c0007t0001g0023a0006c0007t0001g0024others(2): Show | 9 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.97-539G>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 2/38 | chr17 | 69138039 | |||||||
| chr17:69138040 | C | G | 4 | a0003c0009t0001g0258a0006c0010t0001g0255a0006c0010t0001g0256others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.97-540G>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 2/38 | chr17 | 69138040 | |||||||
| chr17:69138284 | C | G | 1 | a0005c0005t0002g0123 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.97-784G>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 2/38 | chr17 | 69138284 | |||||||
| chr17:69138500 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.97-1000G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 2/38 | chr17 | 69138500 | |||||||
| chr17:69138547 | T | A | 2 | a0003c0009t0001g0167a0003c0009t0001g0168 | 2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.97-1047A>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 2/38 | chr17 | 69138547 | |||||||
| chr17:69138548 | C | T | 2 | a0003c0009t0001g0167a0003c0009t0001g0168 | 2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.97-1048G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 2/38 | chr17 | 69138548 | |||||||
| chr17:69138626 | C | T | 1 | a0002c0002t0002g0170 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.97-1126G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 2/38 | chr17 | 69138626 | |||||||
| chr17:69138627 | C | T | 1 | a0002c0002t0002g0170 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.97-1127G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 2/38 | chr17 | 69138627 | |||||||
| chr17:69138656 | G | T | 1 | a0001c0001t0001g0036 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.97-1156C>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 2/38 | chr17 | 69138656 | |||||||
| chr17:69138662 | A | G | 1 | a0007c0006t0002g0035 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.97-1162T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 2/38 | chr17 | 69138662 | |||||||
| chr17:69138666 | G | T | 2 | a0002c0002t0001g0025a0002c0002t0001g0169 | 3 | HG02055.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.97-1166C>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 2/38 | chr17 | 69138666 | |||||||
| chr17:69138747 | G | C | 2 | a0003c0003t0001g0275a0003c0003t0001g0276 | 2 | HG02630.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.97-1247C>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 2/38 | chr17 | 69138747 | |||||||
| chr17:69138775 | C | A | 5 | a0002c0002t0002g0248a0002c0002t0002g0251a0010c0014t0002g0247others(2): Show | 5 | HG02040.hp2 NA19054.hp2 NA19064.hp1 others(2): Show |
intron_variant | MODIFIER | c.97-1275G>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 2/38 | chr17 | 69138775 | |||||||
| chr17:69138787 | C | T | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(145): Show | 176 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.97-1287G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 2/38 | chr17 | 69138787 | |||||||
| chr17:69138791 | G | A | 5 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(2): Show | 5 | HG00099.hp2 HG01346.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-1291C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 2/38 | chr17 | 69138791 | |||||||
| chr17:69138796 | T | C | 1 | a0001c0001t0001g0019 | 2 | NA18955.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.97-1296A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 2/38 | chr17 | 69138796 | |||||||
| chr17:69138883 | G | A | 1 | a0006c0013t0001g0163 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.97-1383C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 2/38 | chr17 | 69138883 | |||||||
| chr17:69139097 | A | G | 28 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0030others(25): Show | 34 | HG00639.hp2 HG01099.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.96+1511T>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 2/38 | chr17 | 69139097 | |||||||
| chr17:69139148 | G | A | 1 | a0013c0016t0001g0159 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.96+1460C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 2/38 | chr17 | 69139148 | |||||||
| chr17:69139264 | G | A | 3 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0120 | 3 | NA18971.hp1 NA19010.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.96+1344C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 2/38 | chr17 | 69139264 | |||||||
| chr17:69139470 | G | C | 1 | a0003c0003t0001g0277 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.96+1138C>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 2/38 | chr17 | 69139470 | |||||||
| chr17:69139474 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.96+1134A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 2/38 | chr17 | 69139474 | |||||||
| chr17:69139476 | G | T | 1 | a0002c0002t0002g0166 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.96+1132C>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 2/38 | chr17 | 69139476 | |||||||
| chr17:69139502 | A | C | 181 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(178): Show | 219 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.96+1106T>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 2/38 | chr17 | 69139502 | |||||||
| chr17:69139526 | G | C | 3 | a0005c0005t0002g0154a0005c0005t0002g0155a0005c0005t0002g0156 | 3 | HG01243.hp1 HG02148.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.96+1082C>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 2/38 | chr17 | 69139526 | |||||||
| chr17:69139539 | T | C | 1 | a0006c0031t0001g0252 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.96+1069A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 2/38 | chr17 | 69139539 | |||||||
| chr17:69139597 | G | C | 1 | a0001c0001t0001g0122 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.96+1011C>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 2/38 | chr17 | 69139597 | |||||||
| chr17:69139661 | G | A | 1 | a0002c0002t0002g0253 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.96+947C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 2/38 | chr17 | 69139661 | |||||||
| chr17:69139803 | T | C | 2 | a0005c0005t0001g0157a0005c0005t0001g0158 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.96+805A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 2/38 | chr17 | 69139803 | |||||||
| chr17:69139839 | T | C | 1 | a0002c0002t0002g0254 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.96+769A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 2/38 | chr17 | 69139839 | |||||||
| chr17:69139864 | G | A | 41 | a0004c0004t0002g0006a0004c0004t0002g0021a0004c0004t0002g0022others(38): Show | 48 | HG00609.hp1 HG00733.hp1 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.96+744C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 2/38 | chr17 | 69139864 | |||||||
| chr17:69139954 | G | T | 1 | a0006c0013t0001g0163 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.96+654C>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 2/38 | chr17 | 69139954 | |||||||
| chr17:69139961 | G | C | 2 | a0005c0005t0001g0157a0005c0005t0001g0158 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.96+647C>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 2/38 | chr17 | 69139961 | |||||||
| chr17:69139961 | G | T | 1 | a0006c0013t0001g0163 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.96+647C>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 2/38 | chr17 | 69139961 | |||||||
| chr17:69140002 | G | A | 147 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(144): Show | 175 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.96+606C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 2/38 | chr17 | 69140002 | |||||||
| chr17:69140012 | G | T | 1 | a0002c0002t0002g0162 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.96+596C>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 2/38 | chr17 | 69140012 | |||||||
| chr17:69140014 | G | T | 1 | a0001c0001t0001g0034 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.96+594C>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 2/38 | chr17 | 69140014 | |||||||
| chr17:69140015 | T | C | 1 | a0013c0016t0001g0159 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.96+593A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 2/38 | chr17 | 69140015 | |||||||
| chr17:69140516 | T | C | 1 | a0005c0005t0002g0160 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.96+92A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 2/38 | chr17 | 69140516 | |||||||
| chr17:69140520 | C | T | 1 | a0004c0004t0002g0033 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.96+88G>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 2/38 | chr17 | 69140520 | |||||||
| chr17:69140759 | A | C | 1 | a0003c0003t0001g0032 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-45-11T>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 1/38 | chr17 | 69140759 | |||||||
| chr17:69140796 | G | A | 1 | a0003c0003t0001g0278 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-45-48C>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 1/38 | chr17 | 69140796 | |||||||
| chr17:69141039 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-45-291A>G | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 1/38 | chr17 | 69141039 | |||||||
| chr17:69141106 | G | T | 147 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(144): Show | 175 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.-45-358C>A | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 1/38 | chr17 | 69141106 | |||||||
| chr17:69141202 | T | A | 28 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0030others(25): Show | 34 | HG00639.hp2 HG01099.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.-45-454A>T | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 1/38 | chr17 | 69141202 | |||||||
| chr17:69141631 | T | G | 1 | a0001c0001t0001g0279 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-46+114A>C | ABCA6 | ENSG00000154262.13 | transcript | ENST00000284425.7 | protein_coding | 1/38 | chr17 | 69141631 |