Source: GWASCAT ×
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 6
rs4917014 0.807 0.360 7 50266267 upstream gene variant T/G snv 0.26 4
rs5010528
HLA-B ; HLA-C
0.827 0.240 6 31273255 intron variant A/G snv 0.15 3
rs77375493
INSL6 ; JAK2
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 3
rs3130501
POU5F1
0.851 0.280 6 31168676 intron variant A/G snv 0.78 3
rs3094188
POU5F1 ; PSORS1C3
0.882 0.200 6 31174468 intron variant C/A;T snv 0.68 3
rs2844665 0.882 0.200 6 31039078 downstream gene variant T/C snv 0.65 2
rs6016348 0.925 0.160 20 40410188 regulatory region variant C/T snv 0.28 2
rs6500265 0.882 0.240 16 49912759 intergenic variant C/G;T snv 0.27 2
rs9888871 0.925 0.160 16 49916730 downstream gene variant G/C snv 0.19 2
rs9469003
LINC01149
0.882 0.160 6 31440051 intron variant T/C snv 0.22 2
rs16957893
LOC107984728
0.925 0.160 15 73437142 intergenic variant G/C snv 4.9E-02 2
rs2734583
SNORD117 ; ATP6V1G2-DDX39B ; DDX39B
0.882 0.240 6 31537703 intron variant A/G snv 0.10 2
rs3130931
TCF19 ; POU5F1
0.925 0.160 6 31167111 5 prime UTR variant T/A;C snv 2
rs17137412
UMAD1
0.925 0.160 7 7761056 intron variant T/G snv 0.17 2
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 1