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Atrial fibrillation

KCNN3 · rs13376333

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Where this position leads

Condition: Atrial Fibrillation (PITX2 Genetic Risk)

rs13376333 Condition: Atrial Fibrillation (PITX2 Genetic Risk) Atrial Fibrillation (PITX2 Genetic Risk) Condition rs13376333 KCNN3

What each result means

C/C Published research associates this genotype with typical/baseline likelihood of Atrial fibrillation — no copies of the reported risk allele. (GWAS Catalog, Nat Genet 2010, PMID:20173747)
C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Atrial fibrillation. (GWAS Catalog, Nat Genet 2010, PMID:20173747)
T/T Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Atrial fibrillation compared to the general population. (GWAS Catalog, Nat Genet 2010, PMID:20173747)

Source: GWAS Catalog, Nat Genet 2010, PMID:20173747

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