Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs34330 0.724 0.280 12 12717761 5 prime UTR variant T/C snv 0.70 15
rs1057519697
ALK
0.776 0.120 2 29220830 missense variant A/C snv 12
rs3136817 0.732 0.280 14 20456275 intron variant T/C snv 0.23 12
rs121917887 0.790 0.120 17 51161744 missense variant A/G snv 6.0E-05 7.0E-05 10
rs4081134 0.790 0.160 14 100855451 non coding transcript exon variant G/A snv 0.29 7
rs369576054 0.807 0.120 4 85994925 missense variant C/T snv 2.8E-05 4.9E-05 6
rs538874513 0.807 0.120 1 3730017 missense variant C/G;T snv 8.2E-06; 8.2E-06 6