Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1799782
XRCC1
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs25489
XRCC1
0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs3213245
XRCC1 ; PINLYP
0.742 0.240 19 43575535 5 prime UTR variant G/A snv 0.65 0.60 13
rs1214285376
XRCC1
0.776 0.200 19 43543490 missense variant G/T snv 4.0E-06 8
rs148611340
XRCC1
0.790 0.120 19 43543621 missense variant G/A;C snv 4.0E-06; 1.2E-05 7
rs199613843
XRCC1
0.807 0.160 19 43551609 synonymous variant C/T snv 4.0E-06 7.0E-06 6
rs2854509
XRCC1
0.807 0.160 19 43570445 intron variant T/G snv 0.80 6
rs2307191
XRCC1
0.827 0.120 19 43553616 missense variant G/A snv 1.2E-03 4.8E-03 5
rs72554204
XRCC1
0.827 0.120 19 43546062 missense variant C/T snv 1.2E-04 1.3E-04 5
rs200842482
XRCC1
0.851 0.120 19 43551592 missense variant C/T snv 1.6E-05 1.4E-05 4
rs2307181
XRCC1
0.851 0.120 19 43544170 synonymous variant G/A;C snv 6.1E-05 4