Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7895833 0.742 0.440 10 67863299 upstream gene variant G/A;C snv 12
rs3846662 0.763 0.280 5 75355259 non coding transcript exon variant A/G snv 0.50 0.58 12
rs972936 0.807 0.200 12 102431143 intron variant T/C snv 0.70 12
rs7483 0.742 0.320 1 109737079 missense variant C/T snv 4.0E-06; 0.35 0.26 11
rs3764650 0.790 0.200 19 1046521 intron variant T/G snv 0.14 9
rs4717806 0.776 0.200 7 73702147 intron variant T/A;C snv 9
rs363050 0.790 0.240 20 10253609 intron variant G/A snv 0.57 8
rs669 0.851 0.080 12 9079672 missense variant T/C snv 0.31 0.33 7
rs2298813 0.790 0.120 11 121522975 missense variant G/A;T snv 7.2E-02; 4.0E-06 7
rs104894103 0.807 0.280 9 32974495 stop gained C/G;T snv 4.0E-06; 1.6E-04 6
rs754203 0.807 0.200 14 99691630 non coding transcript exon variant A/G snv 0.27 6
rs7354779 0.827 0.200 21 44250887 missense variant T/C snv 0.21 6
rs9331888 0.827 0.200 8 27611345 5 prime UTR variant C/G snv 0.35 0.28 5
rs8702 0.851 0.160 14 103686015 3 prime UTR variant C/G snv 0.61 5
rs610932 0.851 0.080 11 60171834 downstream gene variant T/G snv 0.57 5
rs10119 0.925 0.080 19 44903416 3 prime UTR variant G/A snv 0.28 5
rs541458 0.851 0.080 11 86077309 regulatory region variant C/T snv 0.71 4
rs16947151 0.882 0.080 17 49213276 intron variant A/G snv 0.12 4
rs5978930 0.882 0.080 X 8642266 intron variant T/C;G snv 4
rs11887120 0.882 0.080 2 25262866 intron variant C/T snv 0.45 4
rs11767557 0.882 0.080 7 143412046 intron variant T/C snv 0.18 4
rs12752888 0.851 0.160 1 54527266 downstream gene variant T/C snv 0.26 4
rs9357347 0.851 0.080 6 41182853 intergenic variant A/C;T snv 4
rs11637611 0.851 0.160 15 72259371 intron variant C/T snv 0.63 4
rs2070045 0.851 0.080 11 121577381 synonymous variant T/G snv 0.32 0.23 4