Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs5361 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 47
rs6136 0.752 0.440 1 169594713 missense variant T/G snv 8.2E-02 7.5E-02 17
rs1020608562 0.807 0.160 3 46373738 missense variant T/C snv 4.0E-06 9
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs185847354 0.763 0.160 3 186854460 missense variant T/C snv 3.1E-04 7.0E-05 11
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 18
rs3798220
LPA
0.732 0.160 6 160540105 missense variant T/C snv 5.6E-02 3.1E-02 16
rs3861950 0.827 0.160 1 173187153 intron variant T/C snv 0.47 7
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs773297988 0.882 0.080 3 138698965 missense variant T/C snv 4.0E-06 3.5E-05 4
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1799883 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs4821480 0.807 0.160 22 36299201 intron variant G/T snv 0.78 9
rs1232898090 0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs1022113606 0.732 0.280 4 24800161 missense variant G/C snv 1.6E-04 2.1E-05 17
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs2536512 0.752 0.280 4 24799693 missense variant G/A;T snv 0.55 14
rs118204057
LPL
0.732 0.400 8 19954222 missense variant G/A;C snv 1.9E-04 16
rs1801177
LPL
0.742 0.240 8 19948197 missense variant G/A;C snv 1.4E-02; 2.0E-05 14
rs3135506 0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 26