rs11620731

This is a intron variant variant in the COX16 gene.

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GWAS Catalog Trait Associations (2)

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

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 T

OR —

β 0.034

p 7.0e-9

N 94,674

Large GWAS

multi-ancestry

low 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 T

OR —

β 0.042

p 4.0e-10

N 94,674

Large GWAS

multi-ancestry

About COX16

Involved in mitochondrial cytochrome c oxidase assembly. Located in mitochondrial inner membrane. Implicated in mitochondrial complex IV deficiency nuclear type 22. [provided by Alliance of Genome Resources, Jul 2025]

View all COX16 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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