Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2228000
XPC
0.585 0.560 3 14158387 missense variant G/A snv 0.24 0.21 53
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
rs1051730 0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 43
rs401681 0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs1258159645 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 37
rs217727 0.641 0.480 11 1995678 non coding transcript exon variant G/A snv 0.20 34
rs121913483 0.649 0.560 4 1801841 missense variant C/A;G;T snv 4.2E-06; 1.3E-05 31
rs2031920 0.695 0.240 10 133526341 non coding transcript exon variant C/T snv 3.1E-02 20
rs1194611372 0.763 0.320 1 152032679 missense variant A/C snv 9
rs2230641 0.807 0.240 5 87399457 missense variant A/G;T snv 0.18 0.17 8
rs2498801 0.790 0.120 14 104769221 upstream gene variant T/C snv 0.41 7
rs587783064 0.851 0.120 17 7669626 missense variant C/A;T snv 5