rs7499892

This is a intron variant variant in the CETP gene.

GWAS Catalog Trait Associations (26)

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

triglyceride:HDL cholesterol ratio

Allele T
OR 0.17
p
N 402,398
Major Consortium StudyLarge GWAS
European

high density lipoprotein cholesterol measurement

Hoffmann TJ et al. A large electronic-health-record-based genome-wide study of serum lipids. Nature Genetics 50(3):401-413 (2018)
Allele C
OR 0.22
p 1.0e-300
N 94,674
Large GWAS
multi-ancestry
Allele C
OR 0.22
p 1.0e-56
N 22,000
Large GWAS
South Asian
Allele C
OR 0.24
p 4.0e-49
N 4,383
Meta-analysis
multi-ancestry
Allele C
OR 0.23
p 2.0e-8
N 2,317
Large GWAS
East Asian
Allele C
OR 0.22
p 1.0e-15
Large GWAS

triglycerides in IDL measurement

Zoodsma M et al. A genetic map of human metabolism across the allele frequency spectrum. Nature Genetics 57(10):2445-2455 (2025)
Allele T
OR 0.03
p 1.0e-37
N 450,015
Large GWAS
multi-ancestry

total cholesterol measurement

Hoffmann TJ et al. A large electronic-health-record-based genome-wide study of serum lipids. Nature Genetics 50(3):401-413 (2018)
Allele C
OR
β 0.068
p 3.0e-35
N 94,674
Large GWAS
multi-ancestry

cholesteryl esters to total lipids in small HDL percentage

Zoodsma M et al. A genetic map of human metabolism across the allele frequency spectrum. Nature Genetics 57(10):2445-2455 (2025)
Allele T
OR 0.03
p 2.0e-31
N 450,015
Large GWAS
multi-ancestry

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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