Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1161884343
LPL
1.000 0.080 8 19955930 missense variant T/C snv 7.0E-06 1
rs1181582051
LPL
1.000 0.080 8 19956048 missense variant T/C snv 4.0E-06 1
rs118204056
LPL
1.000 0.080 8 19954185 missense variant G/A snv 7.0E-06 1
rs118204059
LPL
1.000 0.080 8 19955876 missense variant T/A snv 1
rs118204061
LPL
1.000 0.080 8 19954240 missense variant T/C snv 1.6E-05 4.2E-05 1
rs118204062
LPL
1.000 0.080 8 19955874 missense variant G/A snv 4.0E-06 1.4E-05 1
rs118204063
LPL
1.000 0.080 8 19953386 missense variant G/A snv 4.0E-06 1
rs118204064
LPL
1.000 0.080 8 19954126 missense variant A/G snv 1
rs118204067
LPL
1.000 0.080 8 19954271 missense variant C/G snv 4.0E-06 1
rs118204069
LPL
1.000 0.080 8 19951856 missense variant T/C snv 7.0E-06 1
rs118204071
LPL
0.925 0.080 8 19959322 missense variant G/A snv 1
rs118204072
LPL
1.000 0.080 8 19954174 missense variant C/G;T snv 4.0E-06 1
rs118204075
LPL
1.000 0.080 8 19954243 missense variant G/A snv 1
rs118204076
LPL
1.000 0.080 8 19954199 missense variant C/G;T snv 1.2E-05 1
rs118204077
LPL
1.000 0.080 8 19955873 missense variant C/T snv 8.0E-06 7.0E-06 1
rs118204078
LPL
0.925 0.080 8 19960935 missense variant C/G snv 1
rs118204079
LPL
1.000 0.080 8 19962126 missense variant G/A snv 1
rs118204080
LPL
1.000 0.080 8 19954333 missense variant T/C snv 2.0E-05 1
rs1409123950
LPL
1.000 0.080 8 19955994 missense variant G/A snv 8.0E-06 1
rs1800011
LPL
1.000 0.080 8 19955927 missense variant G/A;C snv 6.0E-05 1
rs35414700
LPL
1.000 0.080 8 19955901 missense variant T/G snv 1.2E-05 1.4E-05 1
rs373088068
LPL
1.000 0.080 8 19951805 missense variant G/C snv 9.9E-05 1.3E-04 1
rs528243561
LPL
1.000 0.080 8 19954258 missense variant T/A;C snv 3.6E-05 1
rs546542623
LPL
1.000 0.080 8 19959335 missense variant C/T snv 2.0E-05 1
rs568397156
LPL
1.000 0.080 8 19954200 missense variant G/A snv 4.0E-06 1