Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2228001
XPC
0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 60
rs561841803
XPC
1.000 0.160 3 14158384 missense variant G/A snv 8.0E-06 1.4E-05 1
rs2230641 0.807 0.240 5 87399457 missense variant A/G;T snv 0.18 0.17 8
rs4253211 0.882 0.240 10 49470271 missense variant C/G;T snv 7.1E-02; 2.0E-05 3
rs143305574 0.925 0.160 10 49517092 missense variant T/A;C snv 8.0E-06; 6.8E-05 2
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs873601 0.677 0.360 13 102875987 3 prime UTR variant G/A snv 0.59 25
rs2296147 0.695 0.280 13 102846025 5 prime UTR variant T/C snv 0.38 21
rs1047768 0.695 0.320 13 102852167 synonymous variant T/C snv 0.52 0.59 20
rs2094258 0.701 0.280 13 102844409 intron variant C/T snv 0.18 20
rs751402 0.724 0.360 13 102845848 5 prime UTR variant A/G snv 0.76 15
rs2227869 0.790 0.240 13 102862735 missense variant G/A;C snv 4.3E-02 9
rs121434570 0.925 0.160 13 102872397 stop gained G/A;T snv 8.0E-06; 8.0E-06 2
rs121434574 0.925 0.240 13 102852244 missense variant C/A;T snv 4.0E-06 2
rs121434575 0.925 0.240 13 102868152 missense variant T/C snv 2
rs4150351 0.925 0.160 13 102870617 intron variant A/C;T snv 2
rs929424117 0.925 0.160 13 102866645 missense variant T/C snv 4.0E-06 2
rs121434571 1.000 0.160 13 102866687 missense variant C/A;T snv 4.0E-06; 2.4E-05 1
rs121434576 1.000 0.160 13 102868199 missense variant G/A snv 2.4E-05 3.5E-05 1
rs121434577 1.000 0.160 13 102854313 stop gained C/G;T snv 1
rs1244074570 1.000 0.160 13 102866665 stop gained C/G;T snv 4.0E-06 1
rs267607280 1.000 0.160 13 102873283 missense variant G/C snv 1
rs267607281 1.000 0.160 13 102846349 missense variant C/A snv 1
rs752661599 1.000 0.160 13 102872262 frameshift variant A/-;AA delins 1
rs786200919 1.000 0.160 13 102862263 frameshift variant GGAA/- delins 1