Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17577 0.649 0.520 20 46014472 missense variant G/A;C snv 0.16 30
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1799793 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs1799944 0.882 0.080 13 32337326 missense variant A/G snv 5.4E-02 4.5E-02 5
rs1800054
ATM
0.827 0.080 11 108227849 missense variant C/G;T snv 7.1E-03 7
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 37
rs2227982 0.677 0.480 2 241851281 missense variant G/A snv 9.2E-02 4.3E-02 24
rs2228000
XPC
0.585 0.560 3 14158387 missense variant G/A snv 0.24 0.21 53
rs2228001
XPC
0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 60
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs28934578 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 36
rs3136025 0.882 0.080 17 35002030 missense variant G/A snv 6.8E-03 2.7E-02 3
rs34767364
NBN
0.701 0.280 8 89971232 missense variant G/A;C snv 2.5E-03 20
rs36053993 0.677 0.280 1 45331556 missense variant C/T snv 3.0E-03 3.3E-03 24
rs3731249 0.683 0.320 9 21970917 missense variant C/A;G;T snv 2.1E-02 22
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs397514606 0.763 0.320 1 243695714 missense variant C/T snv 13
rs397517132 0.623 0.280 7 55191846 missense variant A/T snv 48
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 264
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 61
rs762846821 0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 56
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 181