Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs61764370 0.662 0.320 12 25207290 3 prime UTR variant A/C snv 6.2E-02 29
rs20575 0.645 0.440 8 23201811 missense variant C/G snv 0.54 0.44 29
rs2234767 0.649 0.280 10 88989499 intron variant G/A;T snv 0.15 30
rs763110 0.653 0.560 1 172658358 upstream gene variant C/T snv 0.49 30
rs17577 0.649 0.520 20 46014472 missense variant G/A;C snv 0.16 31
rs28934571 0.645 0.360 17 7674216 missense variant C/A;G snv 31
rs20576 0.637 0.400 8 23200707 missense variant T/G snv 0.15 0.14 34
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs752742313 0.637 0.320 3 138655502 missense variant C/T snv 1.2E-05 36
rs3834129 0.627 0.560 2 201232809 upstream gene variant AGTAAG/- del 0.48 38
rs746702110 0.627 0.480 3 9756778 missense variant C/T snv 1.2E-05 2.8E-05 38
rs2274223 0.620 0.400 10 94306584 missense variant A/G snv 0.28 0.31 40
rs2228000
XPC
0.585 0.560 3 14158387 missense variant G/A snv 0.24 0.21 53
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs2228001
XPC
0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 60
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1048943 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182