rs12134663
This is a intron variant variant in the C1orf167 gene.
▶GWAS Catalog Trait Associations (1)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (1)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
homocysteine measurement
van Meurs JB et al. “Common genetic loci influencing plasma homocysteine concentrations and their effect on risk of coronary artery disease.” The American Journal of Clinical Nutrition 98(3):668-76 (2013)
Allele A
OR 0.10
p 3.0e-21
N 44,147
Large GWAS
European
About C1orf167
Implicated in coronary artery disease. [provided by Alliance of Genome Resources, Jul 2025]
View all C1orf167 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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