Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs58542926 0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs1800730 0.649 0.480 6 26090957 missense variant A/T snv 1.0E-02 1.0E-02 32
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
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
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
rs11558492 0.827 0.200 1 231272345 missense variant A/G;T snv 0.16 5
rs3194051 0.851 0.200 5 35876172 missense variant A/G snv 0.24 0.28 4
rs3741981 0.882 0.120 12 112911065 missense variant G/A;C snv 3
rs1063303 0.925 0.120 11 5698520 missense variant G/A;C;T snv 4.0E-06; 0.50; 1.6E-05 2
rs267607117 0.925 0.080 8 93780747 missense variant G/T snv 2
rs1060500764 1.000 0.080 15 67181363 missense variant A/G snv 1
rs1430059719 1.000 0.080 20 46012456 missense variant G/C snv 4.0E-06 1
rs900837802 1.000 0.080 2 88595498 missense variant T/C snv 7.0E-06 1
rs1800925 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs236918 0.776 0.160 11 117220893 non coding transcript exon variant G/A;C snv 10
rs14158 0.851 0.160 19 11131368 synonymous variant G/A snv 0.24 0.22 5
rs781521972 1.000 0.080 18 47896706 synonymous variant T/A snv 4.0E-06 1
rs1143627 0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35