rs7813395

This is a intron variant variant in the SAMD12 gene.

GWAS Catalog Trait Associations (1)

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

tumor necrosis factor receptor superfamily member 11B amount

Allele A
OR
β 0.073
p 1.0e-18
N 21,758
Large GWAS
European

About SAMD12

Predicted to be involved in cell surface receptor protein tyrosine kinase signaling pathway. Predicted to be active in cytoplasmic side of plasma membrane. Implicated in familial adult myoclonic epilepsy 1. [provided by Alliance of Genome Resources, Jul 2025]

View all SAMD12 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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