Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 10
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 6
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 6
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 5
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 5
rs10871777 0.925 0.120 18 60184530 intergenic variant A/G snv 0.24 4
rs17700144 1.000 0.080 18 60144750 intron variant G/A snv 0.14 4
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 4
rs4854344 1.000 0.080 2 638144 regulatory region variant G/T snv 0.82 4
rs633715 1.000 0.080 1 177883445 intron variant T/C snv 0.17 4
rs6548238 0.882 0.200 2 634905 TF binding site variant T/C snv 0.85 4
rs7561317 0.925 0.120 2 644953 intergenic variant A/G snv 0.81 4
rs8089364 0.925 0.120 18 60191596 upstream gene variant T/C snv 0.21 4
rs11084753 1.000 0.080 19 33831232 intergenic variant A/C;G;T snv 0.65 3
rs12463617 1.000 0.080 2 629244 regulatory region variant A/C;T snv 3
rs13013484 2 27765954 intergenic variant G/A snv 0.61 3
rs13130484 1.000 0.080 4 45173674 intergenic variant C/A;T snv 3
rs2867125 0.925 0.120 2 622827 intergenic variant T/A;C snv 0.85 3
rs29941 1.000 0.080 19 33818627 downstream gene variant A/G snv 0.70 3
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 3
rs887912 1.000 0.080 2 59075742 intron variant T/C;G snv 3
rs9936833 0.882 0.160 16 86369512 intergenic variant C/T snv 0.64 3
rs10173167 2 646767 intergenic variant G/A snv 0.82 2
rs10188334 2 653874 regulatory region variant C/A;T snv 0.15 2
rs10193244 2 647580 intergenic variant T/C snv 0.77 2