Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs2234767 0.649 0.280 10 88989499 intron variant G/A;T snv 0.15 30
rs7120118 0.716 0.360 11 47264739 intron variant T/C snv 0.38 18
rs2072668 0.732 0.280 3 9756456 intron variant C/G snv 0.28 0.24 14
rs7922612 0.752 0.080 10 94051682 intron variant C/T snv 0.39 14
rs11954856
APC
0.732 0.200 5 112751630 intron variant T/G snv 0.54 12
rs4791171 0.763 0.080 17 65545379 intron variant T/C snv 0.55 11
rs2303426 0.790 0.080 2 47403411 intron variant C/A;G;T snv 1.9E-05; 0.47 8
rs35463555 0.776 0.160 19 50374423 intron variant G/A snv 0.29 8
rs4595552 0.790 0.080 11 125865825 intergenic variant C/G;T snv 7
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs1048943 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs2228001
XPC
0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 60
rs2228000
XPC
0.585 0.560 3 14158387 missense variant G/A snv 0.24 0.21 53
rs2274223 0.620 0.400 10 94306584 missense variant A/G snv 0.28 0.31 40
rs746702110 0.627 0.480 3 9756778 missense variant C/T snv 1.2E-05 2.8E-05 38
rs752742313 0.637 0.320 3 138655502 missense variant C/T snv 1.2E-05 36