Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800206 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
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
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
rs185847354 0.763 0.160 3 186854460 missense variant T/C snv 3.1E-04 7.0E-05 11
rs20455 0.763 0.160 6 39357302 missense variant A/G snv 0.41 0.49 12
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs2229616 0.732 0.200 18 60372043 missense variant C/T snv 1.6E-02 1.6E-02 22
rs2295490 0.724 0.320 20 388261 missense variant A/G;T snv 0.18; 4.0E-06 16
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs2536512 0.752 0.280 4 24799693 missense variant G/A;T snv 0.55 14
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
rs375752214 0.708 0.400 7 150998541 missense variant C/T snv 4.1E-06 4.2E-05 22
rs3798220
LPA
0.732 0.160 6 160540105 missense variant T/C snv 5.6E-02 3.1E-02 16
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs5355 0.742 0.240 1 169726729 missense variant G/A snv 4.5E-02 3.3E-02 14
rs5361 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 47
rs660339 0.695 0.320 11 73978059 missense variant G/A snv 0.41 0.43 24
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157