rs3781370

This is a intron variant variant in the NEURL1 gene.

GWAS Catalog Trait Associations (1)

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

atrial fibrillation

Allele C
OR 0.02
p 1.0e-30
N 1,486,094
Large GWAS
European

About NEURL1

Predicted to enable translation factor activity, non-nucleic acid binding and ubiquitin protein ligase activity. Involved in negative regulation of Notch signaling pathway; negative regulation of cell population proliferation; and positive regulation of apoptotic process. Located in plasma membrane. [provided by Alliance of Genome Resources, Apr 2025]

View all NEURL1 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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