Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs153109 0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs156697 0.672 0.560 10 104279427 missense variant A/G;T snv 0.35 25
rs4925 0.677 0.560 10 104263031 missense variant C/A snv 0.25 0.23 28
rs3218536 0.620 0.440 7 152648922 missense variant C/G;T snv 4.0E-06; 6.4E-02 37
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 39
rs20576 0.637 0.400 8 23200707 missense variant T/G snv 0.15 0.14 34
rs4143815 0.689 0.400 9 5468257 3 prime UTR variant G/C snv 0.23 20
rs2107425 0.732 0.280 11 1999845 intron variant C/T snv 16
rs2304277 0.776 0.280 3 9759396 non coding transcript exon variant G/A snv 0.26 8
rs138213197 0.701 0.240 17 48728343 missense variant C/T snv 1.8E-03 1.6E-03 24
rs874945 0.732 0.240 12 53961667 upstream gene variant C/T snv 0.38 14
rs1046428 0.776 0.200 14 77327940 missense variant T/A;C snv 4.0E-06; 0.81 8
rs80357138 0.763 0.200 17 43094776 missense variant C/T snv 8.0E-06 9