rs7904973

This is a intron variant variant in the C10orf88 gene.

GWAS Catalog Trait Associations (6)

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

low density lipoprotein cholesterol measurement

Allele T
OR 0.02
p 5.0e-38
N 1,320,016
Large GWAS
European
Allele T
OR 0.02
p 1.0e-14
N 297,626
Major Consortium StudyLarge GWAS
multi-ancestry
de Vries PS et al. Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions. American Journal of Epidemiology 188(6):1033-1054 (2019)
Allele T
OR 0.92
p 3.0e-9
N 127,326
Large GWAS
multi-ancestry

total cholesterol measurement

Allele T
OR 0.02
p 1.0e-35
N 1,320,016
Large GWAS
European

mean corpuscular hemoglobin concentration

Verma A et al. Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. Science (new York, N.y.) 385(6706):eadj1182 (2024)
Allele G
OR 0.02
p 2.0e-18
N 407,345
Major Consortium StudyLarge GWAS
European

low density lipoprotein cholesterol measurement, alcohol consumption quality

de Vries PS et al. Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions. American Journal of Epidemiology 188(6):1033-1054 (2019)
Allele T
OR
p 8.0e-10
N 71,394
Large GWAS
multi-ancestry

low density lipoprotein cholesterol measurement, alcohol drinking

de Vries PS et al. Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions. American Journal of Epidemiology 188(6):1033-1054 (2019)
Allele T
OR
p 3.0e-11
N 127,326
Large GWAS
multi-ancestry

Red cell distribution width

Allele G
OR
p 8.0e-48
N 563,352
Large GWAS
multi-ancestry
Verma A et al. Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. Science (new York, N.y.) 385(6706):eadj1182 (2024)
Allele G
OR 0.03
p 2.0e-32
N 380,819
Major Consortium StudyLarge GWAS
European

About C10orf88

Enables ATP hydrolysis activity. Located in mitochondrion. [provided by Alliance of Genome Resources, Jul 2025]

View all C10orf88 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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