Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10920501 0.827 0.120 1 190092815 downstream gene variant A/T snv 0.18 5
rs965384857
LPL
0.827 0.160 8 19954234 missense variant G/A snv 4.0E-06 5
rs7819412 0.827 0.120 8 11187652 intron variant G/A;T snv 6
rs1049673 0.807 0.160 7 80677034 3 prime UTR variant C/G;T snv 7
rs2000813 0.763 0.200 18 49567494 missense variant C/A;T snv 4.0E-06; 0.27; 4.0E-06 0.23 9
rs3732581 0.790 0.120 3 183840614 missense variant C/G;T snv 0.46; 1.2E-05 9
rs1320702652 0.752 0.160 15 43824536 missense variant G/A snv 4.0E-06 11
rs185847354 0.763 0.160 3 186854460 missense variant T/C snv 3.1E-04 7.0E-05 11
rs1761667 0.752 0.320 7 80615623 intron variant G/A snv 0.49 12
rs9282541 0.790 0.160 9 104858554 missense variant G/A snv 1.3E-02 4.4E-03 13
rs2516839 0.732 0.320 1 161043331 5 prime UTR variant C/T snv 0.49 14
rs11066001 0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 15
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 15
rs80356814 0.732 0.320 1 156138697 synonymous variant C/T snv 8.0E-06 15
rs116843064 0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02 16
rs2295490 0.724 0.320 20 388261 missense variant A/G;T snv 0.18; 4.0E-06 16
rs3091244
CRP
0.724 0.280 1 159714875 upstream gene variant G/A;T snv 17
rs16147 0.695 0.400 7 24283791 upstream gene variant T/C snv 0.48 18
rs1800775 0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 18
rs1051931 0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
rs328
LPL
0.732 0.440 8 19962213 stop gained C/G snv 9.2E-02 9.0E-02 19
rs2383207 0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs660339 0.695 0.320 11 73978059 missense variant G/A snv 0.41 0.43 24
rs708272 0.708 0.440 16 56962376 intron variant G/A snv 0.42 0.38 24
rs1041981 0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38 25