Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs1051266 0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 41
rs1232898090 0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs1799883 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36
rs1799889 0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs1927911 0.658 0.640 9 117707776 intron variant A/G snv 0.62 28
rs1799895 0.683 0.360 4 24800212 missense variant C/G snv 2.3E-02 1.2E-02 26
rs2230806 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
rs112735431 0.683 0.320 17 80385145 missense variant G/A;C snv 2.6E-04; 8.0E-06 24
rs2249825 0.695 0.440 13 30463766 5 prime UTR variant G/A;C;T snv 23
rs2383207 0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs2108622 0.742 0.280 19 15879621 missense variant C/T snv 0.27 0.22 20
rs11053646 0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13 18
rs3850641 0.716 0.400 1 173206693 intron variant A/G snv 0.14 17
rs688 0.742 0.400 19 11116926 synonymous variant C/T snv 0.39 0.34 16
rs1042579 0.732 0.240 20 23048087 missense variant G/A;T snv 0.19 16
rs2241883 0.763 0.360 2 88124547 missense variant T/C snv 0.30 0.29 14
rs2536512 0.752 0.280 4 24799693 missense variant G/A;T snv 0.55 14
rs6218 0.732 0.440 12 102399855 3 prime UTR variant A/G snv 2.1E-02 13
rs2227631 0.742 0.200 7 101126257 upstream gene variant A/G snv 0.54 13
rs4918 0.763 0.400 3 186620593 missense variant G/A;C snv 0.67 12
rs3027898 0.752 0.360 X 154010439 downstream gene variant C/A snv 11
rs121918474 0.763 0.320 3 93905799 missense variant T/C snv 2.8E-05 1.4E-05 11
rs12218 0.763 0.280 11 18269774 synonymous variant T/C snv 0.42 0.36 11