Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 37
rs78378222 0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 22
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
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 213
rs369576054 0.807 0.120 4 85994925 missense variant C/T snv 2.8E-05 4.9E-05 6
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1800975
XPA
0.701 0.360 9 97697296 5 prime UTR variant T/C;G snv 0.63; 4.5E-06; 4.5E-06 19