Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1329568 0.882 0.120 9 37037979 upstream gene variant T/A;G snv 6
rs10821944
ARID5B
1.000 0.120 10 62025330 3 prime UTR variant G/T snv 0.66 3
rs10892279 1.000 0.120 11 118741072 intron variant G/A;T snv 0.25 3
rs11893432
STAT4
0.827 0.120 2 191057148 intron variant C/G snv 0.21 3
rs2283790
UBE2L3
0.882 0.120 22 21602364 intron variant A/G snv 0.21 3
rs1049281
HLA-C
1.000 0.120 6 31268790 3 prime UTR variant T/C snv 0.68 2
rs11761528
ZKSCAN5
1.000 0.120 7 99521178 intron variant C/T snv 0.12 2
rs12191877
HLA-B
0.851 0.120 6 31285148 intron variant C/T snv 0.12 2
rs140142800 1.000 0.120 10 61036479 regulatory region variant C/T snv 2.2E-02 2
rs1502644 1.000 0.120 5 3670892 intergenic variant C/A snv 0.85 2
rs1877030 1.000 0.120 17 39583908 intergenic variant T/C snv 0.81 2
rs1953126
PHF19
1.000 0.120 9 120878222 intron variant T/C snv 0.68 2
rs2834512
RCAN1
1.000 0.120 21 34539301 intron variant G/A snv 0.15 2
rs2858310 1.000 0.120 6 32700546 TF binding site variant G/A snv 0.64 2
rs3132947
NOTCH4
1.000 0.120 6 32209005 intron variant G/T snv 0.19 2
rs3781094
GATA3
1.000 0.120 10 8059464 intron variant A/C snv 0.52 2
rs3823418
PSORS1C1
0.925 0.120 6 31133165 intron variant G/A snv 0.23 2
rs4272
CDK6
1.000 0.120 7 92607515 3 prime UTR variant A/G;T snv 2
rs4921283 0.925 0.120 5 160443604 intron variant G/A snv 0.52 2
rs589428
SLC44A4 ; CYP21A2 ; EHMT2 ; LOC107986588 ; EHMT2-AS1
1.000 0.120 6 31880443 non coding transcript exon variant T/G snv 0.77 2
rs6593803
LOC105371230 ; LOC102723321
1.000 0.120 1 147733635 intergenic variant C/T snv 0.22 2
rs6684311 1.000 0.120 1 166516654 intergenic variant C/G snv 0.22 2
rs702873
LINC01185
0.882 0.120 2 60854407 intron variant C/T snv 0.35 2
rs7258015
ICAM3
0.925 0.120 19 10338682 missense variant T/C snv 0.22 0.20 2
rs9267531
LY6G5B ; CSNK2B
0.882 0.120 6 31668965 non coding transcript exon variant A/G snv 7.5E-02 2