Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5880 0.827 0.040 16 56981179 missense variant G/C snv 5.2E-02 3.7E-02 10
rs884164 0.925 0.040 19 4521613 upstream gene variant A/G;T snv 2
rs11234027 0.882 0.080 11 71523061 intron variant G/A snv 0.24 5
rs147377392 0.763 0.120 20 23048144 missense variant A/G snv 1.0E-04 2.8E-04 11
rs544456198 0.790 0.120 19 11116930 missense variant G/T snv 8.0E-06 2.8E-05 9
rs10903323 0.807 0.160 8 10292057 intron variant A/G snv 0.15 8
rs1320702652 0.752 0.160 15 43824536 missense variant G/A snv 4.0E-06 11
rs4717806 0.776 0.200 7 73702147 intron variant T/A;C snv 9
rs752596535 0.752 0.200 19 11105407 stop gained C/A;G;T snv 1.6E-05 14
rs7944926 0.807 0.200 11 71454579 intron variant A/G snv 0.54 7
rs1042579 0.732 0.240 20 23048087 missense variant G/A;T snv 0.19 16
rs1801177
LPL
0.742 0.240 8 19948197 missense variant G/A;C snv 1.4E-02; 2.0E-05 14
rs11053646 0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13 18
rs1800777 0.724 0.280 16 56983407 missense variant G/A snv 3.7E-02 2.8E-02 17
rs2383207 0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs1239681664 0.716 0.320 9 104818690 synonymous variant A/G snv 7.0E-06 15
rs2295490 0.724 0.320 20 388261 missense variant A/G;T snv 0.18; 4.0E-06 16
rs11591147 0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 28
rs12794714 0.708 0.360 11 14892029 synonymous variant G/A snv 0.41 0.35 15
rs1799895 0.683 0.360 4 24800212 missense variant C/G snv 2.3E-02 1.2E-02 26
rs5882 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
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
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs72653706 0.695 0.480 16 16163078 stop gained G/A snv 1.4E-03 1.2E-03 32