Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7219923
GSDMB
0.882 0.160 17 39918265 non coding transcript exon variant C/T snv 0.52 4
rs9303281
GSDMB
0.882 0.160 17 39917793 non coding transcript exon variant G/A snv 0.50 4
rs9303277
IKZF3
0.790 0.240 17 39820216 intron variant C/T snv 0.52 4
rs11557467
ZPBP2
0.851 0.200 17 39872381 missense variant G/T snv 0.45 0.45 4
rs10484561 0.827 0.160 6 32697643 intergenic variant T/G snv 0.13 3
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 3
rs12950743 0.925 0.160 17 39892980 intergenic variant T/C snv 0.45 3
rs13192471 0.925 0.160 6 32703326 downstream gene variant T/C snv 0.19 3
rs2523477 0.925 0.080 6 31392612 downstream gene variant T/C snv 0.10 3
rs2596480 0.925 0.120 6 31458208 intron variant C/G;T snv 3
rs7130588 0.882 0.200 11 76559639 regulatory region variant A/G snv 0.29 3
rs7359623 0.925 0.160 17 39893336 intergenic variant C/T snv 0.44 3
rs8069176 0.882 0.080 17 39900944 downstream gene variant G/A;T snv 3
rs9901146 0.882 0.160 17 39887090 intergenic variant G/A snv 0.45 3
rs9907088 0.925 0.160 17 39878863 downstream gene variant G/A snv 0.39 3
rs17388568
ADAD1
0.827 0.280 4 122408207 intron variant G/A snv 0.20 3
rs1008723
GSDMB
0.925 0.160 17 39910014 intron variant G/C;T snv 3
rs4795400
GSDMB
0.925 0.080 17 39910767 intron variant C/T snv 0.36 3
rs7216389
GSDMB
0.732 0.440 17 39913696 intron variant C/T snv 0.60 3
rs7224129
GSDMB
0.925 0.160 17 39919173 non coding transcript exon variant G/A snv 0.52 3
rs869402
GSDMB
0.925 0.160 17 39911790 intron variant T/A;C snv 3
rs6906021
HLA-DQB1-AS1
0.827 0.320 6 32658534 upstream gene variant T/C snv 0.47 3
rs10445308
IKZF3
0.851 0.240 17 39781794 intron variant C/T snv 0.38 3
rs3816470
IKZF3
0.925 0.160 17 39829548 intron variant A/G snv 0.54 3
rs907091
IKZF3
0.851 0.280 17 39765489 3 prime UTR variant C/T snv 0.47 3