Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs121434569 0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
rs2228001
XPC
0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 60
rs876658657 0.677 0.280 3 37020356 missense variant A/G snv 4.0E-06 25
rs1057519861 0.776 0.080 7 55181398 missense variant T/A snv 15
rs767935771
AXL
0.827 0.080 19 41259690 missense variant T/C snv 1.6E-05 5.6E-05 6
rs3787728 0.851 0.080 21 36071595 intron variant T/C snv 0.74 5