Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs7652589 0.732 0.400 3 122170241 downstream gene variant A/G snv 0.60 13
rs12509595 1.000 0.080 4 80261400 intergenic variant T/C snv 0.23 10
rs267734 0.925 0.120 1 150979001 upstream gene variant T/C snv 0.14 7
rs4014195 0.882 0.200 11 65739351 intergenic variant C/G snv 0.31 7
rs12513649 0.851 0.160 5 173045049 regulatory region variant C/G;T snv 6
rs10109414 1.000 0.080 8 23893638 regulatory region variant C/T snv 0.37 5
rs139401390 0.851 0.120 10 88643382 regulatory region variant A/G snv 1.0E-02 5
rs2823139 1.000 0.080 21 15204463 intron variant G/A snv 0.34 5
rs2453533 1.000 0.080 15 45349027 intergenic variant C/A snv 0.56 4
rs6465825 1.000 0.080 7 77787122 downstream gene variant T/C snv 0.41 4
rs7123489 1.000 0.080 11 65756781 intron variant C/A snv 0.29 4
rs743811 0.882 0.160 22 35396981 upstream gene variant T/A;C snv 4
rs12197043 0.882 0.160 6 149130141 regulatory region variant A/G snv 0.37 3
rs13230625 1.000 0.080 7 1246608 regulatory region variant G/A snv 0.62 3
rs1670754 0.882 0.160 4 32263375 intergenic variant G/A snv 0.24 3
rs1933182 1.000 0.080 1 109457216 intergenic variant A/C snv 0.63 3
rs34861762 1.000 0.080 8 23890907 regulatory region variant C/T snv 0.37 3
rs4897081 0.882 0.160 6 149115402 upstream gene variant G/A;T snv 3
rs8014363 0.882 0.160 14 53964857 downstream gene variant C/T snv 0.61 3
rs9379832 1.000 0.080 6 26185972 downstream gene variant A/G snv 0.26 3
rs10178409 1.000 0.080 2 73628380 downstream gene variant G/T snv 0.26 2
rs1066621 1.000 0.080 3 191708066 regulatory region variant C/T snv 0.39 2
rs11662622 1.000 0.080 18 65592400 intergenic variant A/G snv 0.20 2
rs12137135 0.925 0.080 1 22348728 intergenic variant A/C;G snv 2