Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1064039 0.827 0.200 20 23637790 missense variant C/G;T snv 0.20 6
rs1042579 0.732 0.240 20 23048087 missense variant G/A;T snv 0.19 16
rs12375498 1.000 0.080 9 116187719 synonymous variant C/T snv 0.19 0.17 1
rs1805123 0.724 0.280 7 150948446 missense variant T/A;C;G snv 1.3E-05; 0.18; 8.4E-06 18
rs4244285 0.695 0.360 10 94781859 synonymous variant G/A;C snv 0.18 18
rs4220
FGB
0.925 0.080 4 154570607 missense variant G/A snv 0.17 0.15 6
rs3745601 0.882 0.120 19 10113872 missense variant G/A snv 0.16 0.13 3
rs11053646 0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13 18
rs5361 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 47
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs6125 0.925 0.080 1 169613079 missense variant C/T snv 5.6E-02 5.2E-02 2
rs3798220
LPA
0.732 0.160 6 160540105 missense variant T/C snv 5.6E-02 3.1E-02 16
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs1800730 0.649 0.480 6 26090957 missense variant A/T snv 1.0E-02 1.0E-02 32
rs61688134 0.882 0.080 12 21864476 missense variant C/T snv 7.4E-03 7.5E-03 3
rs41508050 0.882 0.080 14 61738090 missense variant C/T snv 3.8E-03 4.0E-03 4
rs28940579 0.732 0.440 16 3243310 missense variant A/G;T snv 2.2E-03; 4.0E-06 13
rs72653706 0.695 0.480 16 16163078 stop gained G/A snv 1.4E-03 1.2E-03 32
rs34637584 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs184934308 0.925 0.080 3 38575342 synonymous variant G/A snv 4.1E-04 9.1E-05 2
rs61752717 0.583 0.840 16 3243407 missense variant T/A;C snv 2.8E-04 72
rs201698592 0.925 0.080 11 2847916 synonymous variant C/T snv 1.7E-04 2.8E-05 2