Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12527379 1.000 0.080 6 131958700 intron variant G/A snv 0.31 1
rs1371367785 1.000 0.080 11 70206265 missense variant G/A snv 4.0E-06 7.0E-06 1
rs17878467 0.925 0.080 17 78214076 upstream gene variant C/G;T snv 6
rs60745952 0.925 0.080 4 148827842 intron variant T/C snv 0.13 6
rs4135113
TDG
0.925 0.080 12 103982915 missense variant G/A;C;T snv 4.7E-02 5
rs10222633 0.925 0.080 3 122258079 intron variant G/A snv 0.45 4
rs10934578 0.925 0.080 3 122258435 intron variant G/T snv 0.30 4
rs12591359 0.925 0.080 15 51247171 intron variant G/A snv 0.41 4
rs2770150 0.925 0.080 9 117700861 upstream gene variant A/G snv 0.22 4
rs7987649 0.925 0.080 13 28320278 intron variant A/G snv 0.35 4
rs1017621656 0.925 0.080 19 41352923 missense variant A/C;G snv 1.9E-05 3
rs1057519822 0.925 0.080 15 66481818 missense variant T/A snv 3
rs1440032367 0.925 0.080 6 33189169 missense variant G/C snv 7.0E-06 3
rs187960998 0.925 0.080 15 31065098 mature miRNA variant C/T snv 1.2E-05 6.3E-05 3
rs352144 0.925 0.080 3 52227452 intron variant T/G snv 3.7E-02 3
rs4562 0.925 0.080 17 7260420 missense variant A/G snv 0.65 0.70 3
rs4648110 0.925 0.080 4 102612664 intron variant T/A snv 0.22 3
rs63751701 0.925 0.080 3 36993663 stop gained G/A;T snv 3
rs760891242
XPC
0.925 0.080 3 14168309 missense variant G/C snv 4.0E-06 7.0E-06 3
rs774904310 0.925 0.080 9 21971055 frameshift variant C/- delins 3
rs9869263 0.925 0.080 3 190312891 synonymous variant A/C;G;T snv 8.0E-06; 0.83; 4.0E-06 3
rs10450310 0.925 0.080 10 52764898 downstream gene variant G/A snv 0.29 2
rs1060503118 0.925 0.080 7 5987422 missense variant C/T snv 2
rs10958713 0.925 0.080 8 42323198 intron variant C/T snv 0.28 2
rs11625206 0.925 0.080 14 70727436 3 prime UTR variant C/T snv 0.26 2