rs572617131

This variant is located in the ARMC9 gene.

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GWAS Catalog Trait Associations (1)

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

level of UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 7 in blood

Loya H et al. “A scalable variational inference approach for increased mixed-model association power.” Nature Genetics 57(2):461-468 (2025)

Allele T

OR 0.59

p 3.0e-20

N 47,745

Large GWAS

European

About ARMC9

Predicted to be involved in cilium assembly and positive regulation of smoothened signaling pathway. Located in centriole and ciliary basal body. Implicated in Joubert syndrome 30. [provided by Alliance of Genome Resources, Jul 2025]

View all ARMC9 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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