Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs121913255 0.667 0.400 1 114713907 missense variant T/A;G snv 26
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs121913237 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 50
rs121913250 0.683 0.440 1 114716127 missense variant C/A;G;T snv 25
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs401681 0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs121913364 0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06 34
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913227 0.653 0.320 7 140753336 missense variant AC/CT;TT mnv 31
rs121913378 0.776 0.280 7 140753337 missense variant C/A;G;T snv 11
rs121913369 0.790 0.280 7 140753346 missense variant G/A;C snv 4.0E-06 12
rs121913338 0.677 0.400 7 140753354 missense variant T/A;C;G snv 24
rs397516896 0.763 0.360 7 140753355 missense variant C/G;T snv 11
rs121913370 0.763 0.360 7 140753393 missense variant T/C;G snv 10
rs121913355 0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 42
rs121913357 0.742 0.320 7 140781603 stop gained C/A;G;T snv 12
rs121913351 0.776 0.240 7 140781611 missense variant C/A;G;T snv 4.0E-06 9
rs121913348 0.763 0.480 7 140781617 missense variant C/A;G;T snv 20
rs2228001
XPC
0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 60