Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs217727 0.641 0.480 11 1995678 non coding transcript exon variant G/A snv 0.20 34
rs2228000
XPC
0.585 0.560 3 14158387 missense variant G/A snv 0.24 0.21 53
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs1051730 0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 43
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205