Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 18
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 18
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 17
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
rs8067378 0.752 0.240 17 39895095 regulatory region variant A/G snv 0.50 12
rs3135363 0.776 0.360 6 32421871 intergenic variant A/G snv 0.24 8
rs7775055 0.790 0.200 6 32690139 TF binding site variant T/C snv 6.2E-02 7
rs11117433 0.827 0.160 16 85985910 upstream gene variant G/A;C;T snv 6
rs6421571 0.851 0.200 11 118873063 intergenic variant T/A;C snv 6
rs7774434 0.807 0.360 6 32689801 TF binding site variant T/C snv 0.40 6
rs12946510 0.851 0.160 17 39756124 downstream gene variant C/T snv 0.37 5
rs2856683 0.827 0.320 6 32687441 regulatory region variant T/A;C;G snv 0.25 5
rs6933404 0.925 0.280 6 137638098 intergenic variant T/C snv 0.16 5
rs9357152 0.827 0.240 6 32697183 regulatory region variant A/G snv 0.24 5
rs11117432 0.851 0.200 16 85985665 upstream gene variant G/A snv 0.15 4
rs12134279 0.925 0.080 1 197812068 regulatory region variant C/T snv 0.17 4
rs2006996 0.882 0.080 9 114830358 regulatory region variant T/C snv 7.2E-02 4
rs231725 0.851 0.240 2 203875952 downstream gene variant G/A snv 0.38 4
rs4938573 0.851 0.280 11 118871133 regulatory region variant C/T snv 0.79 4
rs9901146 0.882 0.160 17 39887090 intergenic variant G/A snv 0.45 4
rs12950743 0.925 0.160 17 39892980 intergenic variant T/C snv 0.45 3
rs715412 1.000 0.080 11 118813901 regulatory region variant G/A snv 0.17 3
rs7359623 0.925 0.160 17 39893336 intergenic variant C/T snv 0.44 3
rs9907088 0.925 0.160 17 39878863 downstream gene variant G/A snv 0.39 3