| geneid | 26574 |
|---|---|
| ensemblid | ENSG00000275700.6 |
| hgncid | 19235 |
| symbol | AATF |
| name | apoptosis antagonizing transcription factor |
| refseq_nuc | NM_012138.4 |
| refseq_prot | NP_036270.1 |
| ensembl_nuc | ENST00000619387.5 |
| ensembl_prot | ENSP00000477848.1 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 36948954 |
| end | 37056871 |
| strand | + |
| ver | v1.2 |
| region | chr17:36948954-37056871 |
| region5000 | chr17:36943954-37061871 |
| regionname0 | AATF_chr17_36948954_37056871 |
| regionname5000 | AATF_chr17_36943954_37061871 |
| 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 |
|---|
| 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 | annotation | impact | samples | ahapids | achapids | acthapids | actghapids | ac | an | af | len | genename | geneid | featuretype | featureid | transcript_biotype | rank | hgvs_c | hgvs_p | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
chr17:36949770
|
G | A | intron_variant | MODIFIER | HG00735.hp2 HG01106.hp2 HG01109.hp1 others(91): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0003a0002c0004others(5): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(9): Show | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(91): Show | 94 | 245 | 0.3837 | 0 | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 1/11 | c.92-444G>A | ||||||
|
chr17:36950077
|
G | A | intron_variant | MODIFIER | HG00735.hp2 HG01106.hp2 HG01109.hp1 others(71): Show |
a0001a0004a0006 | a0001c0001a0001c0003a0004c0010others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(5): Show | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(71): Show | 74 | 245 | 0.3020 | 0 | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 1/11 | c.92-137G>A | ||||||
|
chr17:36950474
|
T | C | intron_variant | MODIFIER | HG00735.hp1 HG00735.hp2 HG01106.hp2 others(79): Show |
a0001a0003a0004others(1): Show | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(9): Show | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(79): Show | 82 | 245 | 0.3347 | 0 | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 2/11 | c.283+69T>C | ||||||
|
chr17:36951001
|
A | G | intron_variant | MODIFIER | HG00735.hp2 HG01167.hp2 HG01243.hp2 others(36): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(1): Show | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(36): Show | 39 | 245 | 0.1592 | 0 | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 2/11 | c.283+596A>G | ||||||
|
chr17:36952426
|
G | C | intron_variant | MODIFIER | HG00735.hp2 HG01106.hp2 HG01109.hp1 others(84): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0003a0002c0004others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(10): Show | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(84): Show | 87 | 245 | 0.3551 | 0 | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 2/11 | c.284-460G>C | ||||||
|
chr17:36952548
|
A | C | intron_variant | MODIFIER | HG00735.hp2 HG01106.hp2 HG01109.hp1 others(77): Show |
a0001a0003a0004others(1): Show | a0001c0001a0001c0003a0003c0005others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(8): Show | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(77): Show | 80 | 245 | 0.3265 | 0 | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 2/11 | c.284-338A>C | ||||||
|
chr17:36954139
|
G | C | intron_variant | MODIFIER | HG00735.hp2 HG01106.hp2 HG01109.hp1 others(91): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0003a0002c0004others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(10): Show | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(91): Show | 94 | 245 | 0.3837 | 0 | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | c.832+232G>C | ||||||
|
chr17:36955781
|
G | A | intron_variant | MODIFIER | HG00735.hp2 HG01109.hp1 HG01167.hp2 others(43): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(1): Show | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(43): Show | 46 | 245 | 0.1878 | 0 | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | c.832+1874G>A | ||||||
|
chr17:36968270
|
CT | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
a0001a0004 | a0001c0001a0001c0002a0004c0010 | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(6): Show | a0001c0001t0001g0021a0001c0001t0001g0032a0001c0001t0001g0049others(95): Show | 98 | 245 | 0.4000 | -1 | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | c.832+14393delT | INFO_REALIGN_3_PRIME | |||||
|
chr17:36970762
|
G | A | intron_variant | MODIFIER | HG01167.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0054 | 1 | 245 | 0.0041 | 0 | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | c.833-15855G>A | ||||||
|
chr17:36978448
|
G | A | intron_variant | MODIFIER | HG00735.hp2 HG01167.hp2 HG01257.hp2 others(21): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0006a0001c0001t0008 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(21): Show | 24 | 245 | 0.0980 | 0 | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | c.833-8169G>A | ||||||
|
chr17:36986300
|
G | C | intron_variant | MODIFIER | HG00735.hp2 HG01167.hp2 HG01257.hp2 others(21): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0006a0001c0001t0008 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(21): Show | 24 | 245 | 0.0980 | 0 | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 4/11 | c.833-317G>C | ||||||
|
chr17:37001405
|
GAGGA | G | intron_variant | MODIFIER | HG01167.hp1 HG01167.hp2 HG01261.hp1 others(31): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0006a0001c0002t0002others(3): Show | a0001c0001t0001g0014a0001c0001t0001g0026a0001c0001t0001g0038others(31): Show | 34 | 245 | 0.1388 | -4 | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 8/11 | c.1398+10595_1398+10598delGAAG | INFO_REALIGN_3_PRIME | |||||
|
chr17:37009739
|
T | C | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(196): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(17): Show | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(195): Show | 199 | 245 | 0.8122 | 0 | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 8/11 | c.1399-9266T>C | ||||||
|
chr17:37022113
|
CGT | C | intron_variant | MODIFIER | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(90): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(3): Show | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0049others(90): Show | 93 | 245 | 0.3796 | -2 | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 10/11 | c.1547+1137_1547+1138delTG | INFO_REALIGN_3_PRIME | |||||
|
chr17:37023490
|
T | TATTCTTT others(23): Show |
intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(61): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(3): Show | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0023others(61): Show | 64 | 245 | 0.2612 | 30 | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 10/11 | c.1547+2646_1547+2675dupTAAAAAGAGGCATTCTTTTTAAACAGAGTT | INFO_REALIGN_3_PRIME | |||||
|
chr17:37027891
|
C | G | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(17): Show | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(241): Show | 245 | 245 | 1.0000 | 0 | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 10/11 | c.1548-3723C>G | ||||||
|
chr17:37033477
|
C | T | intron_variant | MODIFIER | HG01167.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0054 | 1 | 245 | 0.0041 | 0 | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 11/11 | c.1619+1792C>T | ||||||
|
chr17:37037039
|
C | T | intron_variant | MODIFIER | HG01167.hp2 HG01257.hp1 HG01261.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002 | a0001c0001t0001g0054a0001c0001t0001g0056a0001c0001t0001g0057others(4): Show | 7 | 245 | 0.0286 | 0 | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 11/11 | c.1619+5354C>T | ||||||
|
chr17:37040471
|
T | TA | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(17): Show | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(240): Show | 244 | 245 | 0.9959 | 1 | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 11/11 | c.1619+8796dupA | INFO_REALIGN_3_PRIME | |||||
|
chr17:37049031
|
A | G | intron_variant | MODIFIER | HG01167.hp2 HG01257.hp1 HG01261.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002 | a0001c0001t0001g0054a0001c0001t0001g0056a0001c0001t0001g0057others(4): Show | 7 | 245 | 0.0286 | 0 | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 11/11 | c.1620-7570A>G | ||||||
|
chr17:37051697
|
G | GAC | intron_variant | MODIFIER | HG00280.hp2 HG00621.hp2 HG01106.hp2 others(29): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0002t0002 | a0001c0001t0001g0020a0001c0001t0001g0050a0001c0001t0001g0051others(29): Show | 32 | 245 | 0.1306 | 2 | AATF | ENSG00000275700.6 | transcript | ENST00000619387.5 | protein_coding | 11/11 | c.1620-4873_1620-4872dupAC | INFO_REALIGN_3_PRIME |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| AATF | 0/1 | a0001 | 560 | 233 | 78 | 43 | 80 | 8 | 23 | subcellular location copy fasta | chr17 | 36943954 | 37061871 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| AATF | 0/1 | c0001 | 1683 | 192 | 64 | 35 | 70 | 6 | 16 | copy fasta | chr17 | 36943954 | 37061871 |
| genename | grch38/chm13v2 | thapid | tlen | total | AFR | AMR | EAS | EUR | SAS | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| AATF | 0/0 | t0001 | 380 | 166 | 71 | 31 | 46 | 5 | 13 | copy fasta | chr17 | 36943954 | 37061871 |
| genename | grch38/chm13v2 | ghapid | total | AFR | AMR | EAS | EUR | SAS | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|
| AATF | 0/0 | g0054 | 1 | 0 | 1 | 0 | 0 | 0 | chr17 | 36943954 | 37061871 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| AATF | 0/1 | a0001c0001 | 192 | 64 | 35 | 70 | 6 | 16 | 1683 | copy fasta | chr17 | 36943954 | 37061871 |
| 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 |
acthapid | total | AFR | AMR | EAS | EUR | SAS | tlen | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| AATF | 0/0 | a0001c0001t0001 | 147 | 56 | 30 | 44 | 5 | 12 | 2062 | copy fasta | chr17 | 36943954 | 37061871 |
| 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 |
actghapid | total | AFR | AMR | EAS | EUR | SAS | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|
| AATF | 0/0 | a0001c0001t0001g0054 | 1 | 0 | 1 | 0 | 0 | 0 | chr17 | 36943954 | 37061871 |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 36949216 | + | 1 | -0.9574 | -0.9574 | -0.9574 | 0.0000 | acceptor | a0001c0001t0001g0054 | HG01167.hp2 | HG01167.hp2 | AATF | chr17 | 36943954 | 37061871 |
| 36950214 | + | 2 | 0.9904 | 0.9904 | 0.9904 | 0.0000 | donor | a0001c0001t0001g0054 | HG01167.hp2 | HG01167.hp2 | AATF | chr17 | 36943954 | 37061871 |
| 36950405 | + | 2 | -0.9939 | -0.9939 | -0.9939 | 0.0000 | acceptor | a0001c0001t0001g0054 | HG01167.hp2 | HG01167.hp2 | AATF | chr17 | 36943954 | 37061871 |
| 36952886 | + | 3 | 0.9974 | 0.9974 | 0.9974 | 0.0000 | donor | a0001c0001t0001g0054 | HG01167.hp2 | HG01167.hp2 | AATF | chr17 | 36943954 | 37061871 |
| 36953296 | + | 3 | -0.9970 | -0.9970 | -0.9970 | 0.0000 | acceptor | a0001c0001t0001g0054 | HG01167.hp2 | HG01167.hp2 | AATF | chr17 | 36943954 | 37061871 |
| 36953770 | + | 4 | 0.9417 | 0.9417 | 0.9417 | 0.0000 | donor | a0001c0001t0001g0054 | HG01167.hp2 | HG01167.hp2 | AATF | chr17 | 36943954 | 37061871 |
| 36953907 | + | 4 | -0.9409 | -0.9409 | -0.9409 | 0.0000 | acceptor | a0001c0001t0001g0054 | HG01167.hp2 | HG01167.hp2 | AATF | chr17 | 36943954 | 37061871 |
| 36986617 | + | 5 | 0.9545 | 0.9545 | 0.9545 | 0.0000 | donor | a0001c0001t0001g0054 | HG01167.hp2 | HG01167.hp2 | AATF | chr17 | 36943954 | 37061871 |
| 36986731 | + | 5 | -0.9740 | -0.9740 | -0.9740 | 0.0000 | acceptor | a0001c0001t0001g0054 | HG01167.hp2 | HG01167.hp2 | AATF | chr17 | 36943954 | 37061871 |
| 36988519 | + | 6 | 0.9950 | 0.9950 | 0.9950 | 0.0000 | donor | a0001c0001t0001g0054 | HG01167.hp2 | HG01167.hp2 | AATF | chr17 | 36943954 | 37061871 |
| 36988720 | + | 6 | -0.8064 | -0.8064 | -0.8064 | 0.0000 | acceptor | a0001c0001t0001g0054 | HG01167.hp2 | HG01167.hp2 | AATF | chr17 | 36943954 | 37061871 |
| 36989247 | + | 7 | 0.9985 | 0.9985 | 0.9985 | 0.0000 | donor | a0001c0001t0001g0054 | HG01167.hp2 | HG01167.hp2 | AATF | chr17 | 36943954 | 37061871 |
| 36989411 | + | 7 | -0.9988 | -0.9988 | -0.9988 | 0.0000 | acceptor | a0001c0001t0001g0054 | HG01167.hp2 | HG01167.hp2 | AATF | chr17 | 36943954 | 37061871 |
| 36990774 | + | 8 | 0.9945 | 0.9945 | 0.9945 | 0.0000 | donor | a0001c0001t0001g0054 | HG01167.hp2 | HG01167.hp2 | AATF | chr17 | 36943954 | 37061871 |
| 36990857 | + | 8 | -0.9995 | -0.9995 | -0.9995 | 0.0000 | acceptor | a0001c0001t0001g0054 | HG01167.hp2 | HG01167.hp2 | AATF | chr17 | 36943954 | 37061871 |
| 37019005 | + | 9 | 0.9988 | 0.9988 | 0.9988 | 0.0000 | donor | a0001c0001t0001g0054 | HG01167.hp2 | HG01167.hp2 | AATF | chr17 | 36943954 | 37061871 |
| 37019072 | + | 9 | -0.9980 | -0.9980 | -0.9980 | 0.0000 | acceptor | a0001c0001t0001g0054 | HG01167.hp2 | HG01167.hp2 | AATF | chr17 | 36943954 | 37061871 |
| 37020934 | + | 10 | 0.9922 | 0.9921 | 0.9922 | 0.0000 | donor | a0001c0001t0001g0054 | HG01167.hp2 | HG01167.hp2 | AATF | chr17 | 36943954 | 37061871 |
| 37021014 | + | 10 | -0.9909 | -0.9909 | -0.9909 | 0.0000 | acceptor | a0001c0001t0001g0054 | HG01167.hp2 | HG01167.hp2 | AATF | chr17 | 36943954 | 37061871 |
| 37031614 | + | 11 | 0.9725 | 0.9725 | 0.9725 | 0.0000 | donor | a0001c0001t0001g0054 | HG01167.hp2 | HG01167.hp2 | AATF | chr17 | 36943954 | 37061871 |
| 37031685 | + | 11 | -0.9917 | -0.9917 | -0.9917 | 0.0000 | acceptor | a0001c0001t0001g0054 | HG01167.hp2 | HG01167.hp2 | AATF | chr17 | 36943954 | 37061871 |
| 37056601 | + | 12 | 0.6631 | 0.6631 | 0.6631 | 0.0000 | donor | a0001c0001t0001g0054 | HG01167.hp2 | HG01167.hp2 | AATF | chr17 | 36943954 | 37061871 |
| pos | annotationhgvs_chgvs_p | clinvarid | clnsig | geneinfo | mc | clndisdb | strand strand
|
ahapid ahapid_count
|
chapid chapid count
|
thapid thapid_count
|
ghapid ghapid_count
|
AHAPIDS ahapids
|
ACHAPIDS achapids
|
ACTHAPIDS acthapids
|
ACTGHAPIDS actghapids
|
haplotypeids haplotypeids
|
impact | chr | ref | alt | external |
|---|
| 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 |
|---|