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
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
rs1057519732 0.827 0.160 15 66436824 missense variant C/A;T snv 6
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs121434595 0.708 0.320 1 114716124 missense variant C/A;G;T snv 19
rs121434596 0.677 0.440 1 114716123 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 26
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121913233 0.627 0.520 11 533874 missense variant T/A;C;G snv 37
rs121913255 0.667 0.400 1 114713907 missense variant T/A;G snv 26
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 33
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs121913338 0.677 0.400 7 140753354 missense variant T/A;C;G snv 24
rs121913343 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 44
rs121913355 0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 42
rs121913357 0.742 0.320 7 140781603 stop gained C/A;G;T snv 12
rs121913361 0.807 0.280 7 140753349 missense variant C/A;G;T snv 7
rs121913396 0.732 0.200 3 41224607 missense variant A/C;G;T snv 13
rs121913403 0.683 0.240 3 41224622 missense variant C/A;G;T snv 23
rs121913407 0.763 0.240 3 41224645 missense variant T/C;G snv 12
rs121913409 0.708 0.400 3 41224646 missense variant C/A;G;T snv 21
rs121913499 0.605 0.520 2 208248389 missense variant G/A;C;T snv 51
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs2228001
XPC
0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 60