Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs41274221 0.851 0.160 7 100093577 mature miRNA variant C/T snv 6.4E-05 4.9E-05 6
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs1536309 0.851 0.160 10 102435445 upstream gene variant A/G snv 0.32 7
rs629367 0.776 0.200 11 122146306 intron variant C/A snv 0.88 11
rs11066280 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs1179251 0.763 0.320 12 68251271 intron variant C/G snv 0.18 14
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs6218 0.732 0.440 12 102399855 3 prime UTR variant A/G snv 2.1E-02 13
rs712 0.677 0.360 12 25209618 3 prime UTR variant A/C snv 0.46 24
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs9589207 0.925 0.080 13 91351335 mature miRNA variant G/A;C snv 5.4E-03; 4.0E-06 4
rs1760944 0.672 0.480 14 20454990 non coding transcript exon variant T/C;G snv 26
rs2494752 0.790 0.120 14 104797271 upstream gene variant A/G snv 0.85 10
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs1478604 0.807 0.240 15 39581120 5 prime UTR variant T/C snv 0.40 9
rs3743073 0.807 0.120 15 78617197 intron variant G/T snv 0.61 11
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs115785973 0.925 0.080 17 78357871 3 prime UTR variant C/G;T snv 3