rs577330509

This variant is located in the VRTN gene.

GWAS Catalog Trait Associations (1)

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

Alzheimer disease, family history of Alzheimer’s disease

Willett JDS et al. Identification of 16 novel Alzheimer's disease loci using multi-ancestry meta-analyses. Alzheimer's & Dementia : the Journal of the Alzheimer's Association 21(2):e14592 (2025)
Allele A
OR
p 5.0e-8
N 404,467
Large GWAS
multi-ancestry

About VRTN

Predicted to enable sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. Predicted to be active in chromatin. [provided by Alliance of Genome Resources, Jul 2025]

View all VRTN variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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