Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs217727 0.641 0.480 11 1995678 non coding transcript exon variant G/A snv 0.20 34
rs2228000
XPC
0.585 0.560 3 14158387 missense variant G/A snv 0.24 0.21 53
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 38
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs1047768 0.695 0.320 13 102852167 synonymous variant T/C snv 0.52 0.59 20
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242