Standard

Atrial fibrillation

FBXO32 · rs78332318

Where this position leads

Condition: Atrial Fibrillation (PITX2 Genetic Risk)

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 2018, PMID:29892015)

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 2018, PMID:29892015)

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 2018, PMID:29892015)

Source: GWAS Catalog, Nat Genet 2018, PMID:29892015

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