Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1231202 0.925 0.080 8 47933959 splice region variant T/A;C snv 0.96 2
rs1635498 0.807 0.160 1 241881973 missense variant C/A;G;T snv 0.96 9
rs1801726 0.732 0.280 3 122284985 missense variant G/C snv 0.95 0.92 13
rs2214102 0.925 0.080 7 87600185 5 prime UTR variant T/A;C snv 0.95 2
rs10754339 0.882 0.120 1 117147650 3 prime UTR variant G/A snv 0.88 0.76 3
rs425535 0.925 0.080 4 73998280 synonymous variant T/C snv 0.87 0.80 2
rs1625895 0.752 0.200 17 7674797 non coding transcript exon variant T/A;C;G snv 9.1E-06; 0.86; 4.5E-06 10
rs1997623 0.807 0.160 7 116525306 missense variant A/C;G snv 0.86 9
rs1802904
XRN1 ; ATR
0.925 0.080 3 142449489 synonymous variant C/T snv 0.86 0.89 2
rs1047972 0.716 0.240 20 56386407 missense variant T/C snv 0.85 0.84 19
rs1675126 0.925 0.080 11 62138902 synonymous variant T/C snv 0.84 0.88 3
rs2682818 0.742 0.320 12 80935757 non coding transcript exon variant A/C;T snv 0.83 14
rs1059476 0.925 0.080 17 8205013 missense variant A/G snv 0.83 0.81 2
rs1046428 0.776 0.200 14 77327940 missense variant T/A;C snv 4.0E-06; 0.81 8
rs4149117 0.763 0.360 12 20858546 missense variant T/C;G snv 0.81 15
rs12355840 0.827 0.240 10 133247608 non coding transcript exon variant C/G;T snv 1.1E-04; 0.80 5
rs2479717 0.925 0.080 6 41937436 intron variant T/A snv 0.79 0.81 3
rs1871446 0.925 0.080 10 60794005 3 prime UTR variant A/G snv 0.78 0.75 2
rs1156287 0.925 0.080 17 54999438 missense variant G/A snv 0.78 0.79 2
rs12676 0.827 0.240 3 53823776 missense variant A/C;T snv 0.77 5
rs4245739 0.708 0.360 1 204549714 3 prime UTR variant C/A;G snv 0.77; 6.2E-06 19
rs10901425 0.851 0.200 10 125773956 missense variant A/G snv 0.76 0.78 4
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1883832 0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 48
rs3865014 0.851 0.080 15 69269179 missense variant G/A snv 0.75 0.69 7