Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1049194905 0.925 0.080 3 38604063 synonymous variant A/G snv 2
rs1237080661 0.925 0.080 3 38604780 stop gained A/G;T snv 2.8E-05 2
rs184934308 0.925 0.080 3 38575342 synonymous variant G/A snv 4.1E-04 9.1E-05 2
rs750678689 0.925 0.080 3 38566466 synonymous variant G/A snv 8.0E-06 2.1E-05 2
rs6125 0.925 0.080 1 169613079 missense variant C/T snv 5.6E-02 5.2E-02 2
rs2227721 0.925 0.080 17 28370430 intron variant C/A;T snv 0.12 2
rs2824292 0.925 0.080 21 17414857 regulatory region variant G/A snv 0.47 3
rs61688134 0.882 0.080 12 21864476 missense variant C/T snv 7.4E-03 7.5E-03 3
rs1805120 0.882 0.080 7 150952443 synonymous variant G/A snv 0.30 0.26 3
rs1050286 0.882 0.160 12 10158964 3 prime UTR variant T/C snv 0.40 3
rs3745601 0.882 0.120 19 10113872 missense variant G/A snv 0.16 0.13 3
rs200034939 0.882 0.080 3 38557248 missense variant C/A snv 3.2E-05 3
rs974453 1.000 0.080 12 20737008 intron variant A/G;T snv 3
rs1233347077 0.851 0.160 19 44905894 missense variant G/C snv 7.0E-06 4
rs1187513719 0.851 0.200 10 94780595 missense variant A/G snv 4.0E-06 4
rs41508050 0.882 0.080 14 61738090 missense variant C/T snv 3.8E-03 4.0E-03 4
rs199473244 0.851 0.120 3 38557251 missense variant C/A snv 4
rs762890235 0.827 0.240 X 15578220 missense variant G/T snv 3.8E-05 9.5E-06 5
rs1799943 0.925 0.080 13 32316435 5 prime UTR variant G/A;C;T snv 0.25 5
rs225015 0.882 0.160 14 80201236 3 prime UTR variant G/A snv 0.37 5
rs146052672 0.851 0.160 6 34242693 intron variant -/C delins 5
rs770572030 0.827 0.160 18 49581427 missense variant T/A;C snv 4.0E-06; 4.0E-06 5
rs1805017 0.851 0.240 6 46716485 missense variant C/A;T snv 4.0E-06; 0.31 5
rs11571836 0.827 0.200 13 32399302 3 prime UTR variant A/G;T snv 6
rs1064039 0.827 0.200 20 23637790 missense variant C/G;T snv 0.20 6