Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2227869 0.790 0.240 13 102862735 missense variant G/A;C snv 4.3E-02 9
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs4915076 0.882 0.080 1 107816883 intron variant T/C snv 9.1E-02 3
rs189037
ATM ; NPAT
0.689 0.400 11 108223106 5 prime UTR variant G/A snv 0.49 22
rs1800057
ATM
0.776 0.200 11 108272729 missense variant C/A;G snv 1.7E-02 11
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 39
rs9400239 1.000 6 108656460 5 prime UTR variant T/C snv 0.55 3
rs4946936 0.790 0.160 6 108682118 3 prime UTR variant T/A;C snv 8
rs34677591 0.742 0.120 11 112086941 missense variant G/A snv 7.5E-03 7.0E-03 12
rs11214077 0.752 0.120 11 112087953 missense variant A/G snv 6.6E-03 6.7E-03 12
rs1057519695 0.641 0.520 1 114713907 missense variant TT/CA;CC mnv 35
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs1057519834 0.658 0.480 1 114713908 missense variant TG/CT mnv 31
rs56391007
MET
0.752 0.200 7 116771936 missense variant C/T snv 7.9E-03 9.0E-03 16
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs10808556 0.925 0.080 8 127400902 non coding transcript exon variant C/T snv 0.50 2
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs1447295 0.658 0.400 8 127472793 intron variant A/C;T snv 29
rs2480258 1.000 10 133538596 intron variant T/C snv 0.63 1
rs16962916 0.925 16 13806476 intergenic variant A/C;G snv 2
rs371428527 0.925 3 138737869 missense variant T/C;G snv 1.2E-05 1.4E-05 2
rs3136166 0.925 16 13938236 intron variant T/G snv 0.44 2
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs2228001
XPC
0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 60