Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519833 0.925 0.120 7 148809375 missense variant G/C snv 3
rs11466782 0.925 0.120 5 157494947 intron variant A/G snv 0.10 3
rs1257715362 0.925 0.120 4 85995065 missense variant A/G snv 7.0E-06 3
rs1555525126 0.925 0.120 17 7673749 missense variant T/C snv 3
rs2466571 0.925 0.120 1 207766701 intron variant G/T snv 0.46 3
rs707824 0.925 0.120 6 14636732 intergenic variant T/C snv 0.74 3
rs708486 0.925 0.120 14 52274253 intron variant A/G snv 0.35 3
rs867830180 0.925 0.120 20 63695147 missense variant G/A;T snv 3
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs2230926 0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02 27
rs867329357 0.925 0.120 13 102872275 missense variant G/A snv 4.0E-06 4.9E-05 3
rs28934578 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 47
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs995922697 0.724 0.560 3 49357413 missense variant A/G snv 4.1E-06 15
rs1800975
XPA
0.701 0.360 9 97697296 5 prime UTR variant T/C;G snv 0.63; 4.5E-06; 4.5E-06 19
rs1799793 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs1353428252 0.851 0.120 15 90088681 missense variant A/C snv 8.0E-06 5
rs121913237 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 50
rs535311760 0.925 0.120 1 3730979 missense variant G/A snv 1.2E-05; 8.2E-06 3
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 57
rs8177400 0.882 0.160 11 126292695 missense variant G/A;C;T snv 2.8E-03; 1.2E-05 4
rs1351687973 0.925 0.120 1 3731497 missense variant G/A snv 1.6E-05 3
rs138228187 0.925 0.120 11 126292650 missense variant C/T snv 4.0E-05 1.4E-05 3
rs387907272 0.572 0.520 3 38141150 stop lost T/C snv 5.2E-05 7.0E-06 73