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
rs1801275 0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
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
rs2853676 0.667 0.560 5 1288432 intron variant T/A;C snv 29
rs1057519903 0.683 0.080 1 226064434 missense variant A/T snv 28
rs2071559
KDR
0.667 0.680 4 55126199 upstream gene variant A/G snv 0.53 26
rs1870377
KDR
0.695 0.520 4 55106807 missense variant T/A snv 0.22 0.20 25
rs121918464 0.708 0.440 12 112450406 missense variant G/A;C snv 25
rs6010620 0.701 0.360 20 63678486 intron variant A/C;G snv 21
rs2305948
KDR
0.732 0.400 4 55113391 missense variant C/A;T snv 4.0E-06; 0.11 18
rs281865545 0.695 0.360 17 64377836 missense variant C/G;T snv 18
rs55832599 0.716 0.360 17 7673821 missense variant G/A snv 18