Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs1232898090 0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs855791 0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 38
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
rs1275561861 0.672 0.360 6 29944350 missense variant G/A snv 23
rs641738 0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs1805094 0.716 0.440 1 65610269 missense variant G/C;T snv 0.16; 4.0E-06 16
rs1044498 0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 15
rs368234815 0.742 0.280 19 39248514 frameshift variant TT/G;T delins 15
rs72613567 0.742 0.320 4 87310240 splice donor variant -/A delins 0.22 14
rs773641005 0.742 0.240 16 58723829 missense variant T/C snv 14
rs11932595 0.827 0.160 4 55457430 intron variant A/G;T snv 12
rs2228603 0.790 0.360 19 19219115 missense variant C/A;T snv 2.8E-05; 5.9E-02 12
rs236918 0.776 0.160 11 117220893 non coding transcript exon variant G/A;C snv 10
rs4149313 0.763 0.240 9 104824472 missense variant T/C snv 9
rs13702
LPL
0.925 0.160 8 19966981 3 prime UTR variant T/A;C snv 7
rs10750097 1.000 0.040 11 116793324 upstream gene variant G/A;C snv 6
rs1800234 0.807 0.240 22 46219983 missense variant T/A;C snv 4.0E-06; 1.1E-02 6
rs2454206 0.851 0.160 4 105275794 missense variant A/G;T snv 0.30; 6.4E-06 6