Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs2228001
XPC
0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 60
rs3212986 0.620 0.400 19 45409478 stop gained C/A;G;T snv 0.29; 4.3E-06; 4.3E-06 42
rs2298881 0.653 0.400 19 45423658 intron variant C/A;T snv 25
rs121912654 0.683 0.400 17 7675143 missense variant C/A;T snv 4.0E-05 21
rs1800067 0.716 0.320 16 13935176 missense variant G/A snv 5.6E-02 5.3E-02 17
rs2276466 0.732 0.320 16 13949318 3 prime UTR variant C/A;G snv 15
rs744154 0.763 0.280 16 13921224 intron variant G/C snv 0.23 11
rs1799801 0.807 0.360 16 13948101 synonymous variant T/C snv 0.27 0.25 9
rs147105770 0.776 0.280 16 13935697 missense variant C/G;T snv 1.2E-05; 6.4E-05 8
rs6498486 0.776 0.200 16 13919809 upstream gene variant A/C snv 0.27 8
rs759843019 0.807 0.240 16 13920188 missense variant G/A snv 8.2E-06 7.0E-06 6
rs121913028 0.851 0.400 19 45414870 missense variant G/A;C snv 1.2E-05; 1.6E-05 4
rs121913049 0.851 0.240 16 13947991 missense variant C/G;T snv 4.8E-04 4
rs2020959 0.882 0.200 16 13947765 stop gained C/A;T snv 3.2E-05; 2.4E-05 4
rs397509403 0.851 0.200 16 13928149 missense variant T/C snv 7.0E-06 4
rs1555468482 0.882 0.240 16 13935663 frameshift variant C/- del 3
rs2276465 0.882 0.200 16 13949157 3 prime UTR variant G/A;C snv 3
rs1799802 0.925 0.200 16 13934224 missense variant C/T snv 4.0E-03 4.6E-03 2
rs143305574 0.925 0.160 10 49517092 missense variant T/A;C snv 8.0E-06; 6.8E-05 2
rs74737358
XPC
0.925 0.160 3 14158882 missense variant G/A;T snv 8.1E-06; 2.6E-03 2