Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28934571 0.645 0.360 17 7674216 missense variant C/A;G snv 31
rs7080536 0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 27
rs1127354 0.667 0.400 20 3213196 missense variant C/A;G snv 7.5E-02 26
rs6897932 0.683 0.560 5 35874473 missense variant C/T snv 0.23 0.21 25
rs12785878 0.677 0.520 11 71456403 intron variant G/A;T snv 25
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs12075 0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 22
rs641738 0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs267606959 0.732 0.200 15 89318986 missense variant G/A snv 2.0E-05 19
rs2596542 0.724 0.200 6 31398818 upstream gene variant C/T snv 0.41 18
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 14
rs72613567 0.742 0.320 4 87310240 splice donor variant -/A delins 0.22 14
rs10774671 0.732 0.480 12 112919388 splice acceptor variant G/A;C snv 0.67 14
rs10833 0.776 0.160 4 141733394 3 prime UTR variant T/A;C snv 10
rs4374383 0.776 0.200 2 112013193 intron variant A/G snv 0.58 10
rs236918 0.776 0.160 11 117220893 non coding transcript exon variant G/A;C snv 10
rs1161457931 0.763 0.200 22 37084836 missense variant C/T snv 6.4E-06 9
rs1208663703 0.763 0.200 22 37086414 missense variant T/C snv 5.2E-06 7.0E-06 9
rs3921 0.807 0.240 4 76021790 3 prime UTR variant C/G snv 0.61 8
rs3480 0.807 0.160 1 32862564 3 prime UTR variant G/A snv 0.56 8
rs11558492 0.827 0.200 1 231272345 missense variant A/G;T snv 0.16 5
rs14158 0.851 0.160 19 11131368 synonymous variant G/A snv 0.24 0.22 5
rs16851720 0.827 0.120 3 141744456 intron variant A/C snv 0.21 5
rs17047200 0.827 0.200 4 166008836 intron variant A/T snv 0.18 5
rs10433937 0.882 0.080 4 87308948 intron variant T/A;C;G snv 4