Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs755100942 0.724 0.320 13 49630894 stop gained G/A snv 4.2E-06 17
rs3212986 0.620 0.400 19 45409478 stop gained C/A;G;T snv 0.29; 4.3E-06; 4.3E-06 42
rs1801155
APC
0.649 0.440 5 112839514 missense variant T/A snv 8.0E-06; 2.0E-03 1.2E-03 42
rs5361 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 47
rs746702110 0.627 0.480 3 9756778 missense variant C/T snv 1.2E-05 2.8E-05 38
rs752021744 0.689 0.440 3 138759306 missense variant T/C snv 1.2E-05 29
rs2066827 0.695 0.320 12 12718165 missense variant T/A;C;G snv 1.6E-04; 1.6E-05; 0.26 21
rs34301344 0.689 0.400 13 49630893 stop gained G/A snv 9.7E-03 7.9E-03 22
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
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
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
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
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
rs3803185 0.708 0.320 13 49630889 missense variant T/C;G snv 0.39 19
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs6886 0.925 0.160 2 85394936 missense variant T/A;C snv 0.58 4
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242