Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 12
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
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 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
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 5
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 4
rs10871777 0.925 0.120 18 60184530 intergenic variant A/G snv 0.24 4
rs2191349 1.000 0.080 7 15024684 intergenic variant G/T snv 0.54 4
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 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
rs998584 6 43790159 downstream gene variant C/A snv 0.41 4
rs10885122 1.000 0.080 10 111282335 intergenic variant T/G snv 0.71 3
rs11084753 1.000 0.080 19 33831232 intergenic variant A/C;G;T snv 0.65 3
rs11257655 1.000 0.080 10 12265895 TF binding site variant C/T snv 0.23 3
rs12463617 1.000 0.080 2 629244 regulatory region variant A/C;T snv 3
rs12967135 18 60181790 intergenic variant G/A snv 0.24 3
rs13130484 1.000 0.080 4 45173674 intergenic variant C/A;T snv 3