Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs2228001
XPC
0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 60
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs10069690 0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs3218536 0.620 0.440 7 152648922 missense variant C/G;T snv 4.0E-06; 6.4E-02 37
rs4759314 0.649 0.440 12 53968051 non coding transcript exon variant G/A snv 0.93 31
rs3783553 0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins 26
rs768623239 0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05 26
rs16917496 0.689 0.360 12 123409283 3 prime UTR variant C/G;T snv 21
rs1799950 0.752 0.240 17 43094464 missense variant T/C snv 4.7E-02 4.6E-02 13
rs80357796 0.752 0.240 17 43094464 frameshift variant T/- del 11
rs2660753 0.790 0.240 3 87061524 intergenic variant T/C snv 0.76 9
rs757210 0.807 0.160 17 37736525 intron variant C/G;T snv 6