Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35761398 0.701 0.520 1 23875429 missense variant TT/CC mnv 19
rs879761216 0.732 0.480 1 23875429 frameshift variant TT/C;T delins 14
rs1946518 0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs9275141 0.827 0.240 6 32683340 intergenic variant T/G snv 0.50 6
rs11712165 0.882 0.200 3 119399949 intron variant T/G snv 0.30 5
rs2074404 0.925 0.120 17 46788073 intron variant T/G snv 0.27 4
rs2249937 1.000 0.080 6 159094277 non coding transcript exon variant T/G snv 0.76 3
rs6726160 1.000 0.080 2 60937594 non coding transcript exon variant T/G snv 0.47 3
rs2501432 0.716 0.480 1 23875430 missense variant T/C;G snv 0.62 16
rs1332099 0.724 0.240 10 99538694 downstream gene variant T/C;G snv 14
rs7579944 0.882 0.200 2 30222160 intergenic variant T/C;G snv 5
rs9457515 1.000 0.080 6 158913093 intron variant T/C;G snv 1
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 18
rs12928404 0.724 0.240 16 28835925 splice region variant T/C snv 0.44 0.45 15
rs10822050 0.724 0.240 10 62679011 downstream gene variant T/C snv 0.33 14
rs11839053 0.724 0.240 13 106410694 intergenic variant T/C snv 7.0E-02 14
rs2075184 0.724 0.240 2 102464132 intergenic variant T/C snv 0.78 14
rs6689858 0.724 0.240 1 197406337 intron variant T/C snv 0.39 14
rs7042370 0.724 0.240 9 12785074 intron variant T/C snv 0.58 14
rs7672495 0.724 0.240 4 4990640 regulatory region variant T/C snv 0.21 14
rs1208663703 0.763 0.200 22 37086414 missense variant T/C snv 5.2E-06 7.0E-06 9
rs1738074 0.790 0.320 6 159044945 5 prime UTR variant T/C snv 0.49 9
rs1800693 0.776 0.360 12 6330843 non coding transcript exon variant T/C snv 0.36; 4.0E-06 0.38 9
rs4819388 0.790 0.240 21 44227538 3 prime UTR variant T/C snv 9
rs6651252 0.790 0.200 8 128554935 intron variant T/C snv 0.19 8