Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35866072 0.716 0.360 11 102713373 missense variant T/G snv 6.0E-02 9.8E-02 17
rs34009635 0.716 0.360 11 102713445 missense variant A/G snv 2.5E-03 6.2E-04 17
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs3740393 0.776 0.280 10 102876898 intron variant G/C;T snv 10
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs1326656542 0.776 0.280 13 108210293 missense variant A/T snv 4.0E-06 10
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 39
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs710886 0.763 0.160 8 127014615 intron variant C/T snv 0.37 9
rs16901904 0.790 0.160 8 127015257 intron variant T/C snv 0.27 7
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs12917 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 45
rs402710 0.716 0.320 5 1320607 non coding transcript exon variant C/T snv 0.33 0.38 18
rs401681 0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs2031920 0.695 0.240 10 133526341 non coding transcript exon variant C/T snv 3.1E-02 20
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