rs41411047

This is a intron variant variant in the RNF13 gene.

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GWAS Catalog Trait Associations (1)

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

myocardial infarction

Wakil SM et al. “A genome-wide association study reveals susceptibility loci for myocardial infarction/coronary artery disease in Saudi Arabs.” Atherosclerosis 245:62-70 (2016)

Allele A

OR 1.51

p 1.0e-11

N 4,431

Large GWAS

Greater Middle Eastern (Middle Eastern, North African or Persian)

About RNF13

The protein encoded by this gene contains a RING zinc finger, a motif known to be involved in protein-protein interactions. The specific function of this gene has not yet been determined. Alternatively spliced transcript variants that encode the same protein have been reported. A pseudogene, which is also located on chromosome 3, has been defined for this gene. [provided by RefSeq, Jul 2008]

View all RNF13 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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