rs6060732

This is a intron variant variant in the CNBD2 gene.

GWAS Catalog Trait Associations (1)

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

vitamin K-dependent protein C measurement

Allele T
OR 0.36
p 1.0e-14
N 2,935
Large GWAS
Greater Middle Eastern (Middle Eastern, North African or Persian)

About CNBD2

Predicted to enable cAMP binding activity. Predicted to be involved in spermatogenesis. Predicted to be located in cytosol. [provided by Alliance of Genome Resources, Jul 2025]

View all CNBD2 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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