Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799895 0.683 0.360 4 24800212 missense variant C/G snv 2.3E-02 1.2E-02 26
rs1800888 0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 23
rs2383207 0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs1022113606 0.732 0.280 4 24800161 missense variant G/C snv 1.6E-04 2.1E-05 17
rs1800777 0.724 0.280 16 56983407 missense variant G/A snv 3.7E-02 2.8E-02 17
rs118204057
LPL
0.732 0.400 8 19954222 missense variant G/A;C snv 1.9E-04 16
rs2295490 0.724 0.320 20 388261 missense variant A/G;T snv 0.18; 4.0E-06 16
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
rs1320702652 0.752 0.160 15 43824536 missense variant G/A snv 4.0E-06 11
rs6834314 0.807 0.160 4 87292656 intergenic variant A/G snv 0.24 10
rs4717806 0.776 0.200 7 73702147 intron variant T/A;C snv 9
rs753152 0.882 0.160 17 42761487 intron variant T/G snv 0.12 6