Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs953038635 0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51
rs6318 0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs1258159645 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 37
rs1801028 0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02 24
rs6314 0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02 23
rs1065852 0.695 0.360 22 42130692 missense variant G/A snv 0.21 0.19 19
rs995922697 0.724 0.560 3 49357413 missense variant A/G snv 4.1E-06 15
rs10828317 0.776 0.280 10 22550699 missense variant T/C snv 9
rs1322643228 0.807 0.280 12 104321110 missense variant C/T snv 7.1E-06 6
rs781598341 0.827 0.240 6 159682510 missense variant T/C snv 4.0E-06 5
rs1182593032 0.851 0.200 16 69718516 missense variant A/G snv 4
rs1231813088 0.851 0.160 10 92690015 missense variant C/T snv 4
rs1322425552 0.851 0.160 17 74923048 missense variant G/A snv 4
rs1457049406 0.851 0.200 22 19962555 missense variant C/T snv 4
rs1330075052 0.882 0.160 12 104215828 missense variant T/C snv 1.4E-05 3
rs201934979 0.882 0.160 15 74749838 missense variant C/T snv 8.8E-05; 8.0E-06 1.3E-04 3
rs2230469 0.882 0.160 10 22550699 missense variant T/C snv 0.27 0.24 3
rs1447119000 0.925 0.120 22 42130763 missense variant G/A snv 2
rs767413934 0.925 0.120 11 113424539 missense variant G/A snv 4.0E-06 2
rs3755557 0.807 0.280 3 120096110 non coding transcript exon variant T/A snv 0.14 6
rs905568 0.925 0.120 3 114232449 non coding transcript exon variant C/A;G;T snv 2
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs6277 0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38 36