Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 20
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 19
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 18
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 14
rs889312 0.732 0.360 5 56736057 regulatory region variant C/A snv 0.69 14
rs11065979 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 12
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 12
rs3939286 0.776 0.360 9 6210099 regulatory region variant T/A;C snv 12
rs7927894 0.742 0.320 11 76590272 upstream gene variant C/T snv 0.35 12
rs8067378 0.752 0.240 17 39895095 regulatory region variant A/G snv 0.50 12
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 11
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 10
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 10
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 10
rs6548238 0.882 0.200 2 634905 TF binding site variant T/C snv 0.85 10
rs10759931 0.790 0.360 9 117701869 upstream gene variant G/A;T snv 9
rs1342326 0.790 0.360 9 6190076 intergenic variant A/C snv 0.21 9
rs10995271 0.776 0.280 10 62678726 downstream gene variant G/C snv 0.32 8
rs11236797 0.790 0.200 11 76588605 upstream gene variant C/A snv 0.39 8
rs112401631 0.882 0.120 17 40608272 TF binding site variant T/A snv 1.1E-02 8
rs10983755 0.790 0.320 9 117702392 upstream gene variant G/A snv 3.2E-02 7
rs7775228 0.790 0.360 6 32690302 TF binding site variant T/C snv 0.15 7
rs802734 0.827 0.280 6 127957653 intergenic variant A/G;T snv 7
rs17454584 0.851 0.080 4 122432277 downstream gene variant A/G snv 0.17 6