LPL, lipoprotein lipase, 4023

N. diseases: 290; N. variants: 116
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs268
rs268
Entrez Id: 4023
Gene Symbol: LPL
LPL
CUI: C0010068
Disease:
Coronary heart disease
0.050 GeneticVariation BEFREE Nine loci were statistically associated with incident CHD events in white participants: 9p21 (rs10757278; P=4.7 × 10(-41)), 16q23.1 (rs2549513; P=0.0004), 6p24.1 (rs499818; P=0.0002), 2q36.3 (rs2943634; P=6.7 × 10(-6)), MTHFD1L (rs6922269, P=5.1 × 10(-10)), APOE (rs429358; P=2.7×10(-18)), ZNF627 (rs4804611; P=5.0 × 10(-8)), CXCL12 (rs501120; P=1.4 × 10(-6)) and LPL (rs268; P=2.7 × 10(-17)). 22042884 2011
dbSNP: rs268
rs268
Entrez Id: 4023
Gene Symbol: LPL
LPL
CUI: C0010068
Disease:
Coronary heart disease
0.050 GeneticVariation BEFREE Also, this meta-analysis shows that the LPL Asn291Ser variant is associated with CHD and T2DM. 16741292 2006
dbSNP: rs268
rs268
Entrez Id: 4023
Gene Symbol: LPL
LPL
CUI: C0010068
Disease:
Coronary heart disease
0.050 GeneticVariation BEFREE The multivariate model included 512 men with coronary artery disease from the REGRESS study who were completely genotyped for eight polymorphisms selected in the univariate procedure (ie, APOA1 G(-75)A, ABCA1 C(-477)T, ABCA1 G1051A, APOC3 T3206G, APOE Arg158Cys, LIPC C(-514)T, LPL Asn291Ser and LPL Ser447Stop). 15657615 2005
dbSNP: rs268
rs268
Entrez Id: 4023
Gene Symbol: LPL
LPL
CUI: C0010068
Disease:
Coronary heart disease
0.050 GeneticVariation BEFREE We determined the frequencies of three LPL polymorphisms (D9N, N291S, and S447X) in 899 men from the Veterans Affairs HDL Intervention Trial (VA-HIT), a study that examined the potential benefits of increasing HDL with gemfibrozil in men with established CHD and low high density lipoprotein cholesterol (HDL-C; < or =40 mg/dl), and compared them with those of men without CHD from the Framingham Offspring Study (FOS). 15292370 2004
dbSNP: rs268
rs268
Entrez Id: 4023
Gene Symbol: LPL
LPL
CUI: C0010068
Disease:
Coronary heart disease
0.050 GeneticVariation BEFREE The somewhat different effects of the D9N and N291S polymorphisms on plasma lipids, and the absence of a clear effect of the N291S on CHD, raise the possibility that the effect of 9N carrier status might be mediated through effects on LPL function in addition to those influencing fasting plasma lipids. 11427211 2001