Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9344 0.653 0.480 11 69648142 splice region variant G/A snv 0.45 0.39 34
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs895819 0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
rs187115 0.695 0.320 11 35154612 intron variant T/C snv 0.37 22
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs4938723 0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs1979277 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 45
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs1042028 0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30 30
rs7726159 0.790 0.160 5 1282204 intron variant C/A snv 0.29 10
rs6504950 0.807 0.120 17 54979110 intron variant G/A snv 0.29 7
rs486907 0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 32
rs1051740 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
rs11134527 0.677 0.400 5 168768351 intron variant G/A snv 0.25 24
rs2072668 0.732 0.280 3 9756456 intron variant C/G snv 0.28 0.24 14
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs5743836 0.658 0.440 3 52226766 intron variant A/G snv 0.20 31
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs4646903 0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 36