rs76876329

This is a intron variant variant in the MEIKIN gene.

GWAS Catalog Trait Associations (1)

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

mammographic density percentage

Allele C
OR 3.21
p 3.0e-8
N 27,900
Large GWAS
European

About MEIKIN

Predicted to be involved in meiotic chromosome segregation and meiotic sister chromatid cohesion. Predicted to be located in kinetochore. [provided by Alliance of Genome Resources, Jul 2025]

View all MEIKIN variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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