Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs132770 0.752 0.320 22 41621260 5 prime UTR variant A/G snv 0.83 14
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs5751129 0.752 0.320 22 41619761 intron variant C/T snv 0.69 14
rs762551 0.701 0.400 15 74749576 intron variant C/A snv 0.67 23
rs2228001
XPC
0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 60
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs1056836 0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs401681 0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs4073 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs2241880 0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 37
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1047840 0.708 0.280 1 241878999 missense variant G/A snv 0.36 0.40 19
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
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs7214723 0.882 0.080 17 3872554 missense variant T/C snv 0.45 0.36 4
rs12740674 0.882 0.080 1 68121775 intron variant C/T snv 0.34 4
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 48