Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1051740 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs2234922 0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 42
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1056836 0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs2228001
XPC
0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 60
rs121913482 0.630 0.680 4 1801837 missense variant C/T snv 45
rs121913483 0.649 0.560 4 1801841 missense variant C/A;G;T snv 4.2E-06; 1.3E-05 31
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs401681 0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs953038635 0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs12917 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 45
rs104894228 0.605 0.560 11 534286 missense variant C/A;G;T snv 48
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 73
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
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