Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 9
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 8
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 8
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 8
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 7
rs13130484 1.000 0.080 4 45173674 intergenic variant C/A;T snv 5
rs2867125 0.925 0.120 2 622827 intergenic variant T/A;C snv 0.85 5
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 5
rs633715 1.000 0.080 1 177883445 intron variant T/C snv 0.17 5
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 4
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 4
rs571312 1.000 0.080 18 60172536 intergenic variant C/A snv 0.26 4
rs887912 1.000 0.080 2 59075742 intron variant T/C;G snv 4
rs10871777 0.925 0.120 18 60184530 intergenic variant A/G snv 0.24 3
rs12955983 1.000 0.080 18 60205756 intergenic variant A/G snv 0.20 3
rs29941 1.000 0.080 19 33818627 downstream gene variant A/G snv 0.70 3
rs7374732 1.000 0.080 3 23161963 regulatory region variant C/T snv 0.73 3
rs9552416 13 18737101 downstream gene variant C/A;T snv 3
rs10458787 1.000 0.040 10 4613373 intergenic variant A/C;G snv 2
rs11142387 9 70383416 downstream gene variant A/C snv 0.49 2
rs12463617 1.000 0.080 2 629244 regulatory region variant A/C;T snv 2
rs12714415 2 651430 intergenic variant T/C snv 0.19 2
rs4715210 6 50929538 regulatory region variant C/G;T snv 2
rs4854344 1.000 0.080 2 638144 regulatory region variant G/T snv 0.82 2
rs7561317 0.925 0.120 2 644953 intergenic variant A/G snv 0.81 2