rs61766340

This is a intron variant variant in the C1orf159 gene.

GWAS Catalog Trait Associations (1)

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

level of agrin in blood

Allele A
OR 0.15
p 3.0e-16
N 47,745
Large GWAS
European

About C1orf159

Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]

View all C1orf159 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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