Standard

Prevalent atrial fibrillation

KCNN3 · rs36004974

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Where this position leads

Condition: Atrial Fibrillation (PITX2 Genetic Risk)

rs36004974 Condition: Atrial Fibrillation (PITX2 Genetic Risk) Atrial Fibrillation (PITX2 Genetic Risk) Condition rs36004974 KCNN3

What each result means

A/A Published research associates this genotype with typical/baseline likelihood of Prevalent atrial fibrillation — no copies of the reported risk allele. (GWAS Catalog, Nat Genet 2017, PMID:28416818)
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Prevalent atrial fibrillation. (GWAS Catalog, Nat Genet 2017, PMID:28416818)
G/G Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Prevalent atrial fibrillation compared to the general population. (GWAS Catalog, Nat Genet 2017, PMID:28416818)

Source: GWAS Catalog, Nat Genet 2017, PMID:28416818

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