Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs387906698 0.827 0.040 7 142751919 missense variant C/A;T snv 4.0E-06; 7.2E-05 8
rs61734659 0.790 0.160 7 142774035 missense variant G/A snv 1.4E-02 8
rs748405415 0.790 0.160 7 142773993 stop gained G/A;T snv 8
rs886037774
LPL
0.882 0.120 8 19955993 missense variant T/C snv 7
rs886037775
LPL
0.882 0.120 8 19960948 missense variant A/T snv 7
rs202003805 0.827 0.120 7 142750561 missense variant C/T snv 9.0E-05 6
rs57749775 0.851 0.080 12 52904822 missense variant A/G;T snv 1.7E-03; 4.0E-06 6
rs76371115 0.807 0.160 7 117531041 missense variant A/C;G;T snv 8.0E-06 6
rs121909293 0.851 0.080 1 15445717 missense variant C/T snv 4.4E-03 3.8E-03 5
rs12688220 0.827 0.200 X 107001537 upstream gene variant C/T snv 0.19 5
rs140808909 0.851 0.120 19 44909080 missense variant G/A snv 2.0E-04 5.6E-05 5
rs42490 0.882 0.160 8 89766285 intron variant G/A snv 0.60 5
rs7057398 0.827 0.080 X 106901299 intron variant T/C snv 0.41 5
rs118204082
LPL
0.851 0.120 8 19955863 missense variant C/G;T snv 1.5E-04 4
rs6622126 0.851 0.080 X 106956972 missense variant G/A snv 0.58 4
rs111033567 0.882 0.040 7 142750582 missense variant A/G snv 3
rs111033568 0.882 0.040 7 142751937 missense variant C/G;T snv 2.0E-05 3
rs11971167 0.882 0.160 7 117642528 missense variant G/A;T snv 1.3E-03 3
rs12008279 0.882 0.080 X 106917472 intron variant A/G;T snv 3
rs12014762 0.882 0.080 X 106940440 intron variant C/T snv 0.14 3
rs145844329 0.882 0.120 8 143215486 missense variant G/A;C snv 2.5E-05; 8.5E-04 3
rs149089920
LPL
0.925 0.120 8 19962134 missense variant G/A snv 6.0E-05 2.1E-04 3
rs190853081 0.925 0.080 19 44909083 missense variant G/A snv 2.0E-04 5.6E-05 3
rs3809849 0.882 0.120 17 4555303 missense variant G/C;T snv 0.21; 3.1E-05 3
rs397508139 0.882 0.160 7 117540237 missense variant T/A;C snv 4.0E-06; 4.0E-06 3