Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs11234027 0.882 0.080 11 71523061 intron variant G/A snv 0.24 5
rs12794714 0.708 0.360 11 14892029 synonymous variant G/A snv 0.41 0.35 15
rs1320702652 0.752 0.160 15 43824536 missense variant G/A snv 4.0E-06 11
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1800777 0.724 0.280 16 56983407 missense variant G/A snv 3.7E-02 2.8E-02 17
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
rs72653706 0.695 0.480 16 16163078 stop gained G/A snv 1.4E-03 1.2E-03 32
rs751141 0.732 0.400 8 27516348 missense variant G/A snv 0.12 0.10 16
rs1801177
LPL
0.742 0.240 8 19948197 missense variant G/A;C snv 1.4E-02; 2.0E-05 14
rs5882 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs1042579 0.732 0.240 20 23048087 missense variant G/A;T snv 0.19 16
rs11591147 0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 28
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs5880 0.827 0.040 16 56981179 missense variant G/C snv 5.2E-02 3.7E-02 10
rs544456198 0.790 0.120 19 11116930 missense variant G/T snv 8.0E-06 2.8E-05 9
rs4717806 0.776 0.200 7 73702147 intron variant T/A;C snv 9
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306