rs11076176

This variant is located in the CETP gene.

GWAS Catalog Trait Associations (12)

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

high density lipoprotein cholesterol measurement

Allele T
OR 0.13
p 2.0e-22
N 18,341
Large GWAS
multi-ancestry
Allele T
OR 0.05
p 3.0e-17
N 115,082
Large GWAS
European
Allele T
OR 0.05
p 3.0e-14
N 88,329
Large GWAS
European

fatty acid amount

Allele G
OR
p 8.0e-18
N 128,922
Large GWAS
European

triglycerides to total lipids in IDL percentage

Zoodsma M et al. A genetic map of human metabolism across the allele frequency spectrum. Nature Genetics 57(10):2445-2455 (2025)
Allele G
OR 0.02
p 9.0e-15
N 450,015
Large GWAS
multi-ancestry

triglyceride measurement, high density lipoprotein cholesterol measurement

Riveros-Mckay F et al. The influence of rare variants in circulating metabolic biomarkers. Plos Genetics 16(3):e1008605 (2020)
Allele T
OR 0.15
p 2.0e-11
N 7,142
Large GWAS
European

ClinVar annotation

Benign★★★
2 submitters1 publication
View on ClinVar →

About CETP

The protein encoded by this gene is found in plasma, where it is involved in the transfer of cholesteryl ester from high density lipoprotein (HDL) to other lipoproteins. Defects in this gene are a cause of hyperalphalipoproteinemia 1 (HALP1). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2013]

View all CETP variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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