| geneid | 5243 |
|---|---|
| ensemblid | ENSG00000085563.15 |
| hgncid | 40 |
| symbol | ABCB1 |
| name | ATP binding cassette subfamily B member 1 |
| refseq_nuc | NM_001348946.2 |
| refseq_prot | NP_001335875.1 |
| ensembl_nuc | ENST00000622132.5 |
| ensembl_prot | ENSP00000478255.1 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 87503017 |
| end | 87600884 |
| strand | - |
| ver | v1.2 |
| region | chr7:87503017-87600884 |
| region5000 | chr7:87498017-87605884 |
| regionname0 | ABCB1_chr7_87503017_87600884 |
| regionname5000 | ABCB1_chr7_87498017_87605884 |
| chr:pos | ref | alt | af | annotation | impact | samples | AHAPIDS | ACHAPIDS | ACTHAPIDS | ACTGHAPIDS | ac | an | len | genename | geneid | featuretype | featureid | transcript_biotype | rank | hgvs_c | hgvs_p | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status |
|---|
| chr:pos | ref | alt | af | annotation | impact | samples | ahapids | achapids | acthapids | actghapids | ac | an | len | genename | geneid | featuretype | featureid | transcript_biotype | rank | hgvs_c | hgvs_p | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status |
|---|
| genename | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
ahapid | alen | total | AFR | AMR | EAS | EUR | SAS | aseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| ABCB1 | 1/0 | a0002 | 1280 | 74 | 4 | 12 | 38 | 4 | 15 | subcellular location copy fasta | chr7 | 87498017 | 87605884 |
| genename | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
chapid | clen | total | AFR | AMR | EAS | EUR | SAS | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| ABCB1 | 1/0 | c0002 | 3843 | 66 | 3 | 10 | 37 | 4 | 11 | copy fasta | chr7 | 87498017 | 87605884 |
| genename | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
achapid | total | AFR | AMR | EAS | EUR | SAS | clen | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| ABCB1 | 1/0 | a0002c0002 | 66 | 3 | 10 | 37 | 4 | 11 | 3843 | copy fasta | chr7 | 87498017 | 87605884 |
Click to load Haplotype QTL data...
| pos | S. Strand |
E# Exon Number |
max | median | min | diff | type | haplotypeid | max_hap_list | min_hap_list | symbol | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 87600755 | - | 1 | -0.7143 | -0.7061 | -0.6748 | 0.0395 | acceptor | a0002c0002 | HG00621.hp2 HG00735.hp2 HG03831.hp1 HG03831.hp2 NA18982.hp2 others(2): Show |
NA18991.hp2 | ABCB1 | chr7 | 87498017 | 87605884 |
| 87600117 | - | 2 | -0.9986 | -0.9983 | -0.9983 | 0.0003 | acceptor | a0002c0002 | homoSapiens_grch38.hp1 | HG01192.hp2 | ABCB1 | chr7 | 87498017 | 87605884 |
| 87600190 | - | 2 | 0.9914 | 0.9901 | 0.9900 | 0.0014 | donor | a0002c0002 | homoSapiens_grch38.hp1 | HG02135.hp2 | ABCB1 | chr7 | 87498017 | 87605884 |
| 87595766 | - | 3 | -0.9681 | -0.9673 | -0.9663 | 0.0018 | acceptor | a0002c0002 | NA18984.hp2 | HG00621.hp2 | ABCB1 | chr7 | 87498017 | 87605884 |
| 87595814 | - | 3 | 0.9717 | 0.9715 | 0.9699 | 0.0019 | donor | a0002c0002 | NA18984.hp2 | HG00621.hp2 | ABCB1 | chr7 | 87498017 | 87605884 |
| 87585512 | - | 4 | -0.9994 | -0.9994 | -0.9993 | 0.0001 | acceptor | a0002c0002 | HG02886.hp1 | homoSapiens_grch38.hp1 | ABCB1 | chr7 | 87498017 | 87605884 |
| 87585680 | - | 4 | 0.9976 | 0.9975 | 0.9973 | 0.0003 | donor | a0002c0002 | NA18986.hp2 | homoSapiens_grch38.hp1 | ABCB1 | chr7 | 87498017 | 87605884 |
| 87570172 | - | 5 | -0.9725 | -0.9646 | -0.9628 | 0.0097 | acceptor | a0002c0002 | NA19077.hp2 | HG03654.hp2 | ABCB1 | chr7 | 87498017 | 87605884 |
| 87570223 | - | 5 | 0.9574 | 0.9567 | 0.9337 | 0.0237 | donor | a0002c0002 | NA19065.hp1 | homoSapiens_grch38.hp1 | ABCB1 | chr7 | 87498017 | 87605884 |
| 87566785 | - | 6 | -0.9492 | -0.9376 | -0.9335 | 0.0157 | acceptor | a0002c0002 | homoSapiens_grch38.hp1 | HG01175.hp2 | ABCB1 | chr7 | 87498017 | 87605884 |
| 87566976 | - | 6 | 0.8347 | 0.8127 | 0.7974 | 0.0373 | donor | a0002c0002 | NA19007.hp2 | HG01175.hp2 | ABCB1 | chr7 | 87498017 | 87605884 |
| 87566070 | - | 7 | -0.9588 | -0.9578 | -0.9537 | 0.0051 | acceptor | a0002c0002 | HG01516.hp1 HG02165.hp2 NA18946.hp2 |
homoSapiens_grch38.hp1 | ABCB1 | chr7 | 87498017 | 87605884 |
| 87566241 | - | 7 | 0.9910 | 0.9906 | 0.9903 | 0.0007 | donor | a0002c0002 | NA19007.hp2 | HG01175.hp2 | ABCB1 | chr7 | 87498017 | 87605884 |
| 87561263 | - | 8 | -0.9861 | -0.9846 | -0.9845 | 0.0016 | acceptor | a0002c0002 | NA18946.hp2 | HG00408.hp1 HG01993.hp1 HG02300.hp1 NA19077.hp2 |
ABCB1 | chr7 | 87498017 | 87605884 |
| 87561387 | - | 8 | 0.9751 | 0.9750 | 0.9735 | 0.0016 | donor | a0002c0002 | HG03704.hp2 | NA19090.hp1 | ABCB1 | chr7 | 87498017 | 87605884 |
| 87553761 | - | 9 | -0.9964 | -0.9960 | -0.9958 | 0.0006 | acceptor | a0002c0002 | NA18946.hp2 | HG00544.hp1 | ABCB1 | chr7 | 87498017 | 87605884 |
| 87553932 | - | 9 | 0.9923 | 0.9918 | 0.9917 | 0.0007 | donor | a0002c0002 | HG01192.hp2 HG02056.hp1 NA18973.hp2 NA19004.hp1 |
HG01517.hp2 NA18968.hp1 |
ABCB1 | chr7 | 87498017 | 87605884 |
| 87550725 | - | 10 | -0.9962 | -0.9962 | -0.9960 | 0.0002 | acceptor | a0002c0002 | NA20805.hp1 | NA18946.hp2 | ABCB1 | chr7 | 87498017 | 87605884 |
| 87550838 | - | 10 | 0.9888 | 0.9883 | 0.9868 | 0.0020 | donor | a0002c0002 | NA18946.hp2 | NA18963.hp1 | ABCB1 | chr7 | 87498017 | 87605884 |
| 87550468 | - | 11 | -0.8816 | -0.8807 | -0.8763 | 0.0053 | acceptor | a0002c0002 | NA19001.hp2 NA19074.hp2 NA19083.hp2 NA19088.hp1 |
HG01517.hp2 NA18968.hp1 |
ABCB1 | chr7 | 87498017 | 87605884 |
| 87550578 | - | 11 | 0.9031 | 0.9016 | 0.8997 | 0.0033 | donor | a0002c0002 | NA20805.hp1 | HG03704.hp2 | ABCB1 | chr7 | 87498017 | 87605884 |
| 87550171 | - | 12 | -0.7985 | -0.7944 | -0.7936 | 0.0050 | acceptor | a0002c0002 | NA18946.hp2 | NA18963.hp1 | ABCB1 | chr7 | 87498017 | 87605884 |
| 87550296 | - | 12 | 0.8461 | 0.8427 | 0.8424 | 0.0036 | donor | a0002c0002 | NA18946.hp2 | NA18963.hp1 | ABCB1 | chr7 | 87498017 | 87605884 |
| 87549851 | - | 13 | -0.9977 | -0.9976 | -0.9976 | 0.0001 | acceptor | a0002c0002 | NA18991.hp2 | NA20805.hp1 | ABCB1 | chr7 | 87498017 | 87605884 |
| 87550054 | - | 13 | 0.9947 | 0.9946 | 0.9945 | 0.0002 | donor | a0002c0002 | NA18946.hp2 | homoSapiens_grch38.hp1 | ABCB1 | chr7 | 87498017 | 87605884 |
| 87549348 | - | 14 | -0.9953 | -0.9951 | -0.9934 | 0.0020 | acceptor | a0002c0002 | NA18991.hp2 | NA20805.hp1 | ABCB1 | chr7 | 87498017 | 87605884 |
| 87549518 | - | 14 | 0.9902 | 0.9898 | 0.9890 | 0.0012 | donor | a0002c0002 | homoSapiens_grch38.hp1 | NA20805.hp1 | ABCB1 | chr7 | 87498017 | 87605884 |
| 87545863 | - | 15 | -0.9992 | -0.9992 | -0.9992 | 0.0000 | acceptor | a0002c0002 | NA18969.hp1 NA18991.hp2 |
HG02056.hp1 NA18986.hp2 |
ABCB1 | chr7 | 87498017 | 87605884 |
| 87546024 | - | 15 | 0.9996 | 0.9996 | 0.9995 | 0.0001 | donor | a0002c0002 | HG02056.hp1 | homoSapiens_grch38.hp1 | ABCB1 | chr7 | 87498017 | 87605884 |
| 87544823 | - | 16 | -0.9803 | -0.9799 | -0.9796 | 0.0007 | acceptor | a0002c0002 | NA18940.hp2 | HG01167.hp2 | ABCB1 | chr7 | 87498017 | 87605884 |
| 87544999 | - | 16 | 0.9980 | 0.9980 | 0.9980 | 0.0000 | donor | a0002c0002 | HG00408.hp1 HG00544.hp1 HG00558.hp1 HG00621.hp2 HG01070.hp2 others(47): Show |
HG01167.hp2 HG04204.hp1 NA18940.hp2 NA18984.hp2 |
ABCB1 | chr7 | 87498017 | 87605884 |
| 87544129 | - | 17 | -0.9708 | -0.9695 | -0.9658 | 0.0050 | acceptor | a0002c0002 | NA18940.hp2 | HG01167.hp2 | ABCB1 | chr7 | 87498017 | 87605884 |
| 87544275 | - | 17 | 0.9813 | 0.9810 | 0.9801 | 0.0012 | donor | a0002c0002 | NA18940.hp2 | HG01167.hp2 | ABCB1 | chr7 | 87498017 | 87605884 |
| 87541357 | - | 18 | -0.9334 | -0.9327 | -0.8968 | 0.0366 | acceptor | a0002c0002 | HG04204.hp1 | HG01167.hp2 | ABCB1 | chr7 | 87498017 | 87605884 |
| 87541464 | - | 18 | 0.9594 | 0.9522 | 0.9269 | 0.0325 | donor | a0002c0002 | NA18940.hp2 | HG01167.hp2 | ABCB1 | chr7 | 87498017 | 87605884 |
| 87539268 | - | 19 | -0.9881 | -0.9877 | -0.9869 | 0.0012 | acceptor | a0002c0002 | HG00735.hp2 HG01516.hp1 HG01517.hp2 HG03491.hp1 HG03669.hp2 others(1): Show |
HG01167.hp2 | ABCB1 | chr7 | 87498017 | 87605884 |
| 87539345 | - | 19 | 0.9886 | 0.9881 | 0.9869 | 0.0018 | donor | a0002c0002 | HG01358.hp1 | HG01167.hp2 | ABCB1 | chr7 | 87498017 | 87605884 |
| 87536458 | - | 20 | -0.9946 | -0.9938 | -0.9937 | 0.0009 | acceptor | a0002c0002 | HG00544.hp1 HG02165.hp2 |
HG01257.hp2 HG03831.hp2 |
ABCB1 | chr7 | 87498017 | 87605884 |
| 87536541 | - | 20 | 0.9803 | 0.9802 | 0.9784 | 0.0018 | donor | a0002c0002 | HG00558.hp1 HG02015.hp1 NA18940.hp2 NA19004.hp1 NA19090.hp1 |
HG00544.hp1 HG02165.hp2 |
ABCB1 | chr7 | 87498017 | 87605884 |
| 87531294 | - | 21 | -0.9993 | -0.9993 | -0.9991 | 0.0002 | acceptor | a0002c0002 | HG00735.hp2 HG01070.hp2 HG01515.hp2 HG01516.hp1 HG01517.hp2 others(9): Show |
HG03490.hp2 NA18973.hp2 |
ABCB1 | chr7 | 87498017 | 87605884 |
| 87531497 | - | 21 | 0.9957 | 0.9954 | 0.9953 | 0.0004 | donor | a0002c0002 | HG03017.hp1 | HG01175.hp2 | ABCB1 | chr7 | 87498017 | 87605884 |
| 87520776 | - | 22 | -0.7994 | -0.7934 | -0.7886 | 0.0108 | acceptor | a0002c0002 | HG00558.hp1 | NA18970.hp1 NA18973.hp2 NA18982.hp2 NA18992.hp2 NA19010.hp1 others(1): Show |
ABCB1 | chr7 | 87498017 | 87605884 |
| 87520876 | - | 22 | 0.8658 | 0.8604 | 0.8549 | 0.0109 | donor | a0002c0002 | HG00558.hp1 | NA18970.hp1 NA18973.hp2 NA18982.hp2 NA18992.hp2 NA19010.hp1 others(1): Show |
ABCB1 | chr7 | 87498017 | 87605884 |
| 87519326 | - | 23 | -0.9372 | -0.9365 | -0.9304 | 0.0068 | acceptor | a0002c0002 | HG00558.hp1 | NA19001.hp2 | ABCB1 | chr7 | 87498017 | 87605884 |
| 87519466 | - | 23 | 0.8897 | 0.8883 | 0.8861 | 0.0036 | donor | a0002c0002 | HG00558.hp1 | NA18986.hp2 | ABCB1 | chr7 | 87498017 | 87605884 |
| 87516509 | - | 24 | -0.9971 | -0.9968 | -0.9967 | 0.0004 | acceptor | a0002c0002 | HG00544.hp1 HG03654.hp2 |
NA20300.hp2 | ABCB1 | chr7 | 87498017 | 87605884 |
| 87516665 | - | 24 | 0.9981 | 0.9981 | 0.9980 | 0.0001 | donor | a0002c0002 | NA19001.hp2 | HG00544.hp1 HG03654.hp2 |
ABCB1 | chr7 | 87498017 | 87605884 |
| 87515231 | - | 25 | -0.9935 | -0.9925 | -0.9924 | 0.0011 | acceptor | a0002c0002 | NA19056.hp1 | NA18986.hp2 | ABCB1 | chr7 | 87498017 | 87605884 |
| 87515428 | - | 25 | 0.9994 | 0.9994 | 0.9994 | 0.0000 | donor | a0002c0002 | HG00544.hp1 HG03654.hp2 NA19056.hp1 |
NA20300.hp2 | ABCB1 | chr7 | 87498017 | 87605884 |
| 87509275 | - | 26 | -0.9993 | -0.9993 | -0.9993 | 0.0000 | acceptor | a0002c0002 | HG00621.hp2 | HG00408.hp1 HG00544.hp1 HG00558.hp1 HG00735.hp2 HG01070.hp2 others(58): Show |
ABCB1 | chr7 | 87498017 | 87605884 |
| 87509481 | - | 26 | 0.9989 | 0.9988 | 0.9988 | 0.0000 | donor | a0002c0002 | homoSapiens_grch38.hp1 | HG00621.hp2 HG01167.hp2 HG03831.hp1 NA20905.hp2 |
ABCB1 | chr7 | 87498017 | 87605884 |
| 87505897 | - | 27 | -0.9671 | -0.9572 | -0.9528 | 0.0143 | acceptor | a0002c0002 | HG00735.hp2 | HG01516.hp1 HG01517.hp2 |
ABCB1 | chr7 | 87498017 | 87605884 |
| 87506043 | - | 27 | 0.9587 | 0.9583 | 0.9435 | 0.0152 | donor | a0002c0002 | NA18964.hp2 | HG01175.hp2 | ABCB1 | chr7 | 87498017 | 87605884 |
| 87504449 | - | 28 | 0.8393 | 0.8017 | 0.7562 | 0.0830 | donor | a0002c0002 | HG01175.hp2 | HG01516.hp1 HG01517.hp2 |
ABCB1 | chr7 | 87498017 | 87605884 |
| CHR:POS | annotationhgvs_chgvs_p | disease trait-log10podds or beta | AHAPIDS ahapids
|
ACHAPIDS achapids
|
ACTHAPIDS acthapids
|
ACTGHAPIDS actghapids
|
haplotypeids haplotypeids
|
study | initial sample size/replication sample size | report genes | mapped gene | strongest snp risk allele | strand strand
|
impact | chr | ref | alt |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
chr7:87540386
|
c.2319+971T>G | Alpha electroencephalogram power0.1 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0004a0002c0002t0001g0173 | HG01070.hp2 HG01515.hp2 HG03831.hp2 |
Genome-Wide Scan for Five Brain Oscillatory Phenot others(57): Show |
191 European ancestry individuals/ | NR | ABCB1 | rs12720066-? | - | MODIFIER | chr7 | A | C |
|
chr7:87571151
|
c.287-928A>T | Cerebral microbleeds0.86 | a0001a0002a0003a0004a0007others(11): Show | a0001c0001a0001c0003a0001c0005a0001c0006a0001c0018others(20): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0001t0004a0001c0001t0005others(55): Show | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0060a0001c0001t0001g0063a0001c0001t0001g0065others(266): Show | HG00140.hp1 HG00280.hp1 HG00323.hp2 HG00408.hp1 HG00423.hp1 others(270): Show |
Association of common genetic variants with brain others(45): Show |
3,321 European ancestry cases, 42 Chinese ancestry others(185): Show |
ABCB1 | ABCB1 | rs6950978-A | - | MODIFIER | chr7 | T | A |
|
chr7:87590165
|
c.118-4485C>G | Chickenpox0.0603 | a0001a0002a0003a0006a0008others(3): Show | a0001c0001a0001c0003a0001c0005a0001c0006a0001c0025others(10): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0001t0010a0001c0001t0015others(25): Show | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(103): Show | HG00280.hp1 HG00408.hp1 HG00408.hp2 HG00544.hp1 HG00558.hp1 others(107): Show |
Genome-wide association and HLA region fine-mappin others(70): Show |
107,769 European ancestry cases, 15,982 European a others(17): Show |
NR | ABCB1 | rs13229143-? | - | MODIFIER | chr7 | G | C |
|
chr7:87501034
|
c.*3209T>G | Gallstone disease0.85 | a0001a0002a0003a0006a0009others(2): Show | a0001c0001a0001c0003a0001c0005a0001c0006a0002c0002others(7): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0005a0001c0001t0010a0001c0001t0015others(15): Show | a0001c0001t0002g0082a0001c0001t0002g0083a0001c0001t0002g0138a0001c0001t0002g0216a0001c0001t0002g0240others(79): Show | HG00323.hp2 HG00423.hp1 HG00423.hp2 HG00544.hp2 HG00597.hp2 others(81): Show |
Genome-wide analysis identifies gallstone-suscepti others(65): Show |
43,639 European ancestry cases, 506,798 European a others(44): Show |
ABCB4 - ABCB1 | rs7802555-C | - | MODIFIER | chr7 | A | C | |
|
chr7:87574963
|
c.287-4740G>A | Persistent chemotherapy-induced alopecia in breast cancerothers(21): Show | a0001a0002a0003a0004a0005others(12): Show | a0001c0001a0001c0003a0001c0005a0001c0006a0001c0018others(24): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0001t0004a0001c0001t0005others(53): Show | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0063a0001c0001t0001g0068others(250): Show | HG00280.hp1 HG00408.hp1 HG00408.hp2 HG00438.hp1 HG00438.hp2 others(257): Show |
Association Between ABCB1 Genetic Variants and Per others(66): Show |
51 European ancestry cases, 122 European ancestry others(66): Show |
ABCB1 | ABCB1 | rs1202179-C | - | MODIFIER | chr7 | C | T |
|
chr7:87502107
|
c.*2136A>G | Alanine aminotransferase levels | a0001a0002a0003a0004a0006others(8): Show | a0001c0001a0001c0003a0001c0005a0001c0006a0002c0002others(13): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004a0001c0001t0005a0001c0001t0007others(33): Show | a0001c0001t0001g0068a0001c0001t0001g0265a0001c0001t0001g0283a0001c0001t0001g0287a0001c0001t0001g0288others(114): Show | HG00140.hp1 HG00323.hp1 HG00323.hp2 HG00423.hp1 HG00423.hp2 others(116): Show |
Analysis across Taiwan Biobank, Biobank Japan, and others(73): Show |
92,615 Taiwanese ancestry individuals/ | ABCB4 - ABCB1 | rs12539997-? | - | MODIFIER | chr7 | T | C | |
|
chr7:87503600
|
c.*643G>A | Phospholipids to total lipids ratio in small HDLothers(14): Show | a0001a0002a0003a0004a0006others(4): Show | a0001c0001a0001c0003a0001c0005a0001c0006a0002c0002others(9): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0005a0001c0001t0008a0001c0001t0009others(22): Show | a0001c0001t0002g0082a0001c0001t0002g0083a0001c0001t0002g0138a0001c0001t0002g0216a0001c0001t0002g0240others(91): Show | HG00323.hp2 HG00423.hp1 HG00423.hp2 HG00544.hp2 HG00597.hp2 others(93): Show |
Genome-wide characterization of circulating metabo others(15): Show |
4,435 East Asian ancestry individuals, 11,340 Sout others(68): Show |
ABCB1 | rs1055302-T | - | MODIFIER | chr7 | C | T | |
|
chr7:87504050
|
c.*193A>G | Cholelithiasis0.19965225 | a0001a0002a0003a0006a0009others(1): Show | a0001c0001a0001c0003a0001c0005a0001c0006a0002c0002others(6): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0005a0001c0001t0010a0001c0001t0019others(15): Show | a0001c0001t0002g0082a0001c0001t0002g0083a0001c0001t0002g0138a0001c0001t0002g0216a0001c0001t0002g0240others(81): Show | HG00323.hp2 HG00423.hp1 HG00423.hp2 HG00544.hp2 HG00597.hp2 others(83): Show |
A scalable variational inference approach for incr others(36): Show |
394,626 European ancestry individuals/ | ABCB1 | rs3842-C | - | MODIFIER | chr7 | T | C |