rs3916027

This variant is located in the LPL gene.

GWAS Catalog Trait Associations (16)

Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.

metabolic syndrome

Allele G
OR 0.16
p 6.0e-33
N 107,230
Large GWAS
East Asian

triglycerides in medium LDL measurement

Karjalainen MK et al. Genome-wide characterization of circulating metabolic biomarkers. Nature 628(8006):130-138 (2024)
Allele A
OR 0.05
p 3.0e-25
N 136,016
Large GWAS
multi-ancestry

triglyceride measurement

Allele A
OR 0.21
p 1.0e-23
N 5,630
Large GWAS

level of phospholipid transfer protein in blood

Allele A
OR 0.05
p 2.0e-18
N 47,745
Large GWAS
European

ClinVar annotation

Benign★★★
2 submitters1 publication
View on ClinVar →

About LPL

LPL encodes lipoprotein lipase, which is expressed in heart, muscle, and adipose tissue. LPL functions as a homodimer, and has the dual functions of triglyceride hydrolase and ligand/bridging factor for receptor-mediated lipoprotein uptake. Severe mutations that cause LPL deficiency result in type I hyperlipoproteinemia, while less extreme mutations in LPL are linked to many disorders of lipoprotein metabolism. [provided by RefSeq, Jul 2008]

View all LPL variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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