Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 20
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 19
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 17
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 15
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 13
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 12
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 11
rs6548238 0.882 0.200 2 634905 TF binding site variant T/C snv 0.85 10
rs2867125 0.925 0.120 2 622827 intergenic variant T/A;C snv 0.85 8
rs11142387 9 70383416 downstream gene variant A/C snv 0.49 7
rs13130484 1.000 0.080 4 45173674 intergenic variant C/A;T snv 7
rs571312 1.000 0.080 18 60172536 intergenic variant C/A snv 0.26 7
rs633715 1.000 0.080 1 177883445 intron variant T/C snv 0.17 7
rs7561317 0.925 0.120 2 644953 intergenic variant A/G snv 0.81 7
rs10871777 0.925 0.120 18 60184530 intergenic variant A/G snv 0.24 6
rs11084753 1.000 0.080 19 33831232 intergenic variant A/C;G;T snv 0.65 6
rs29941 1.000 0.080 19 33818627 downstream gene variant A/G snv 0.70 6
rs4854344 1.000 0.080 2 638144 regulatory region variant G/T snv 0.82 6
rs8089364 0.925 0.120 18 60191596 upstream gene variant T/C snv 0.21 6
rs887912 1.000 0.080 2 59075742 intron variant T/C;G snv 6
rs9936833 0.882 0.160 16 86369512 intergenic variant C/T snv 0.64 6
rs2331841 1.000 0.080 18 60161404 upstream gene variant G/A snv 0.43 5
rs713586 0.925 0.160 2 24935139 intergenic variant T/C snv 0.58 5
rs10458787 1.000 0.040 10 4613373 intergenic variant A/C;G snv 4