Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs1866389 0.790 0.080 5 80065442 missense variant G/C snv 0.17 0.17 9
rs201058276
F7
0.776 0.240 13 113118731 missense variant G/A;C snv 4.8E-05; 4.0E-06 11
rs2043211 0.653 0.480 19 48234449 missense variant A/T snv 0.33 0.29 29
rs20455 0.763 0.160 6 39357302 missense variant A/G snv 0.41 0.49 12
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs2230806 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
rs2295490 0.724 0.320 20 388261 missense variant A/G;T snv 0.18; 4.0E-06 16
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs3135506 0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 26
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs3732581 0.790 0.120 3 183840614 missense variant C/G;T snv 0.46; 1.2E-05 9
rs375752214 0.708 0.400 7 150998541 missense variant C/T snv 4.1E-06 4.2E-05 22
rs3812316 0.763 0.240 7 73606007 missense variant C/G snv 0.10 9.4E-02 14
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs41507953 0.790 0.280 8 27500988 missense variant A/G snv 8.7E-02 0.13 10
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
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs4961 0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 27
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223