Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4759314 0.649 0.440 12 53968051 non coding transcript exon variant G/A snv 0.93 31
rs9915936 0.827 0.120 17 65537671 synonymous variant T/C snv 0.90 0.90 5
rs2057482 0.701 0.440 14 61747130 3 prime UTR variant T/C snv 0.84 0.80 21
rs3787016 0.677 0.280 19 1090804 intron variant A/G snv 0.78 24
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
rs1862626 0.708 0.280 5 56737113 regulatory region variant G/T snv 0.68 17
rs7003908 0.716 0.320 8 47858141 intron variant C/A snv 0.66 16
rs2228001
XPC
0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 60
rs1047768 0.695 0.320 13 102852167 synonymous variant T/C snv 0.52 0.59 20
rs7931342 0.689 0.360 11 69227030 intergenic variant T/G snv 0.58 20
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs213950 0.716 0.320 7 117559479 missense variant G/A snv 0.47 0.57 16
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs1058808 0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 27
rs1056836 0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 28
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs28360071 0.708 0.240 5 83142293 intron variant GATGAGGAAACTAACTCTCAGTGGTGTTTA/- delins 0.48 18
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131