Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs874945 0.732 0.240 12 53961667 upstream gene variant C/T snv 0.38 14
rs1042028 0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30 30
rs2234922 0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 42
rs9282861 0.658 0.440 16 28606193 missense variant C/T snv 31
rs12917 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 45
rs2228001
XPC
0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 60
rs104894228 0.605 0.560 11 534286 missense variant C/A;G;T snv 48
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs121913483 0.649 0.560 4 1801841 missense variant C/A;G;T snv 4.2E-06; 1.3E-05 31
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
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs1799793 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs401681 0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs1056836 0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs121913482 0.630 0.680 4 1801837 missense variant C/T snv 45
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs1051740 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106