Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs72653706 0.695 0.480 16 16163078 stop gained G/A snv 1.4E-03 1.2E-03 32
rs11591147 0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 28
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs1799895 0.683 0.360 4 24800212 missense variant C/G snv 2.3E-02 1.2E-02 26
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
rs5880 0.827 0.040 16 56981179 missense variant G/C snv 5.2E-02 3.7E-02 10
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs11053646 0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13 18
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs751141 0.732 0.400 8 27516348 missense variant G/A snv 0.12 0.10 16
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
rs1042579 0.732 0.240 20 23048087 missense variant G/A;T snv 0.19 16
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs12794714 0.708 0.360 11 14892029 synonymous variant G/A snv 0.41 0.35 15
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs5882 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246