Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2057482 0.701 0.440 14 61747130 3 prime UTR variant T/C snv 0.84 0.80 21
rs1570360 0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs2228001
XPC
0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 60
rs1927911 0.658 0.640 9 117707776 intron variant A/G snv 0.62 28
rs1946518 0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs1143627 0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs1800682 0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 32
rs1927914 0.732 0.520 9 117702447 upstream gene variant G/A snv 0.52 14
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs1056836 0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1076064 0.851 0.160 5 149732603 intron variant A/G snv 0.47 4
rs3798577 0.742 0.320 6 152099995 3 prime UTR variant T/C snv 0.45 16
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs864745 0.763 0.320 7 28140937 intron variant T/C snv 0.41 12
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1047840 0.708 0.280 1 241878999 missense variant G/A snv 0.36 0.40 19