Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3815087
PSORS1C1
0.851 0.200 6 31125810 5 prime UTR variant G/A snv 0.25 7
rs9469003
LINC01149
0.882 0.160 6 31440051 intron variant T/C snv 0.22 5
rs5010528
HLA-B ; HLA-C
0.827 0.240 6 31273255 intron variant A/G snv 0.15 4
rs4917014 0.807 0.360 7 50266267 upstream gene variant T/G snv 0.26 3
rs3130501
POU5F1
0.851 0.280 6 31168676 intron variant A/G snv 0.78 3
rs2844665 0.882 0.200 6 31039078 downstream gene variant T/C snv 0.65 2
rs2734583
SNORD117 ; ATP6V1G2-DDX39B ; DDX39B
0.882 0.240 6 31537703 intron variant A/G snv 0.10 2
rs3094188
POU5F1 ; PSORS1C3
0.882 0.200 6 31174468 intron variant C/A;T snv 0.68 1