Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 11
rs998584 6 43790159 downstream gene variant C/A snv 0.41 11
rs3865188 0.790 0.320 16 82617112 intergenic variant A/G;T snv 10
rs6548238 0.882 0.200 2 634905 TF binding site variant T/C snv 0.85 10
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 9
rs9942416 5 75741470 intergenic variant C/G snv 0.53 9
rs12967135 18 60181790 intergenic variant G/A snv 0.24 8
rs2145272 20 6645571 intergenic variant G/A;T snv 8
rs2867125 0.925 0.120 2 622827 intergenic variant T/A;C snv 0.85 8
rs7923837 0.882 0.160 10 92722160 intergenic variant G/A;T snv 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
rs10132280 14 25458973 intergenic variant C/A snv 0.37 6
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
rs12513649 0.851 0.160 5 173045049 regulatory region variant C/G;T snv 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
rs645040 3 136207780 upstream gene variant G/T snv 0.77 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
rs1884897 20 6632185 regulatory region variant A/G;T snv 5