Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs505151 0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 18
rs7698623 4 87834676 intron variant T/A;C snv 6.1E-05; 0.94 2
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs562556 0.827 0.280 1 55058564 missense variant G/A snv 0.86 0.83 8
rs1613662 0.851 0.120 19 55025227 missense variant G/A snv 0.85 0.83 8
rs5128 0.925 0.080 11 116832924 3 prime UTR variant G/C snv 0.84 0.87 8
rs13190036 5 177310719 non coding transcript exon variant A/G snv 0.83 0.89 1
rs1051931 0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1926447 0.807 0.440 13 46055809 missense variant A/G snv 0.74 0.77 11
rs1801253 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 34
rs1799883 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1800389
WRN
8 31067041 synonymous variant C/T snv 0.71 0.67 1
rs4948550 10 58828793 missense variant T/C snv 0.71 0.64 1
rs1042034 0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 15
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs4917 0.790 0.160 3 186619924 missense variant T/C snv 0.68 0.68 9
rs4918 0.763 0.400 3 186620593 missense variant G/A;C snv 0.67 12
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs1801020 1.000 0.040 5 177409531 5 prime UTR variant A/G snv 0.65 0.67 8
rs17465637 0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 11
rs415895 11 9748015 missense variant C/G snv 0.62 0.61 6
rs5882 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35