Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
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 214
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 96
rs121913499 0.605 0.520 2 208248389 missense variant G/A;C;T snv 51
rs118101777 0.614 0.280 15 90087472 missense variant C/T snv 2.0E-03 1.6E-03 42
rs55819519 0.627 0.400 17 7673751 missense variant C/A;G;T snv 1.6E-04 1.3E-04 40
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 39
rs1057519903 0.683 0.080 1 226064434 missense variant A/T snv 28
rs6010620 0.701 0.360 20 63678486 intron variant A/C;G snv 21
rs779707422 0.763 0.280 8 38417331 missense variant G/A;T snv 4.0E-06 12
rs371409680 0.790 0.120 17 7673772 missense variant C/G;T snv 4.0E-05 7.0E-06 10
rs773442580
EGF
0.851 0.080 4 109913367 missense variant T/C;G snv 4.0E-06 7
rs1476157710 0.925 0.040 12 48970460 missense variant T/C snv 4.1E-06 1.4E-05 3
rs766727892 0.925 0.040 10 113151107 missense variant G/A snv 1.2E-05 7.0E-06 3
rs867657798 0.925 0.040 18 55631366 missense variant G/A;C snv 1.4E-05 3
rs868162712 0.925 0.040 18 55279598 missense variant G/A snv 3