Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1048943 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 39
rs20576 0.637 0.400 8 23200707 missense variant T/G snv 0.15 0.14 34
rs4925 0.677 0.560 10 104263031 missense variant C/A snv 0.25 0.23 28
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1051740 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs156697 0.672 0.560 10 104279427 missense variant A/G;T snv 0.35 25
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246