Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34301344 0.689 0.400 13 49630893 stop gained G/A snv 9.7E-03 7.9E-03 22
rs3803185 0.708 0.320 13 49630889 missense variant T/C;G snv 0.39 19
rs755100942 0.724 0.320 13 49630894 stop gained G/A snv 4.2E-06 17
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 39
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913366 0.763 0.400 7 140753345 missense variant A/C;T snv 12
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs11571833 0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 43
rs555607708 0.667 0.360 22 28695869 frameshift variant G/- del 2.0E-03 1.8E-03 33
rs121913403 0.683 0.240 3 41224622 missense variant C/A;G;T snv 23
rs28931589 0.695 0.240 3 41224613 missense variant G/A;C;T snv 17
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs112445441 0.658 0.400 12 25245347 missense variant C/A;G;T snv 32
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs121913530 0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs2227982 0.677 0.480 2 241851281 missense variant G/A snv 9.2E-02 4.3E-02 24
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 33
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101