Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs328
rs328
LPL
0.732 0.440 8 19962213 stop gained C/G snv 9.2E-02 9.0E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 6 2007 2019
dbSNP: rs13702
rs13702
LPL
0.925 0.160 8 19966981 3 prime UTR variant T/A;C snv
High density lipoprotein measurement
0.800 1.000 3 2011 2018
dbSNP: rs13702
rs13702
LPL
0.925 0.160 8 19966981 3 prime UTR variant T/A;C snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 2 2011 2018
dbSNP: rs264
rs264
LPL
0.882 0.080 8 19955669 intron variant G/A snv 0.14
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.800 1.000 2 2013 2018
dbSNP: rs268
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02
High density lipoprotein measurement
0.800 1.000 2 2012 2019
dbSNP: rs268
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 2 2012 2019
dbSNP: rs326
rs326
LPL
8 19961928 intron variant A/G snv 0.37
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 2 2008 2019
dbSNP: rs326
rs326
LPL
8 19961928 intron variant A/G snv 0.37
High density lipoprotein measurement
0.800 1.000 2 2012 2019
dbSNP: rs328
rs328
LPL
0.732 0.440 8 19962213 stop gained C/G snv 9.2E-02 9.0E-02
High density lipoprotein measurement
0.800 1.000 2 2008 2019
dbSNP: rs15285
rs15285
LPL
1.000 0.040 8 19967156 3 prime UTR variant C/T snv 0.36
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 1 2011 2019
dbSNP: rs268
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.800 1.000 1 2012 2012
dbSNP: rs295
rs295
LPL
1.000 0.040 8 19958727 intron variant A/C snv 0.28
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.800 1.000 1 2011 2011
dbSNP: rs301
rs301
LPL
0.925 0.160 8 19959423 intron variant T/C snv 0.24 0.26
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.800 1.000 1 2011 2011
dbSNP: rs325
rs325
LPL
8 19961817 intron variant T/C snv 9.0E-02
High density lipoprotein measurement
0.800 1.000 1 2010 2019
dbSNP: rs325
rs325
LPL
8 19961817 intron variant T/C snv 9.0E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 1 2008 2019
dbSNP: rs3289
rs3289
LPL
8 19965681 3 prime UTR variant T/C snv 4.0E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 1 2012 2019
dbSNP: rs7016529
rs7016529
LPL
8 19949120 intron variant T/C snv 8.4E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 1 2012 2018
dbSNP: rs7016529
rs7016529
LPL
8 19949120 intron variant T/C snv 8.4E-02
High density lipoprotein measurement
0.800 1.000 1 2012 2018
dbSNP: rs328
rs328
LPL
0.732 0.440 8 19962213 stop gained C/G snv 9.2E-02 9.0E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.710 1.000 1 2011 2016
dbSNP: rs13702
rs13702
LPL
0.925 0.160 8 19966981 3 prime UTR variant T/A;C snv
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 3 2012 2012
dbSNP: rs264
rs264
LPL
0.882 0.080 8 19955669 intron variant G/A snv 0.14
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 3 2009 2013
dbSNP: rs12679834
rs12679834
LPL
8 19962922 intron variant T/C snv 9.4E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 2 2012 2012
dbSNP: rs264
rs264
LPL
0.882 0.080 8 19955669 intron variant G/A snv 0.14
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 2 2012 2013
dbSNP: rs264
rs264
LPL
0.882 0.080 8 19955669 intron variant G/A snv 0.14
High density lipoprotein measurement
0.700 1.000 2 2012 2013
dbSNP: rs268
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 2 2012 2012