Standard

Atrial fibrillation

PITX2 · rs79399769

Share:

Where this position leads

Condition: Atrial Fibrillation (PITX2 Genetic Risk)

rs79399769 Condition: Atrial Fibrillation (PITX2 Genetic Risk) Atrial Fibrillation (PITX2 Genetic Risk) Condition rs79399769 PITX2

What each result means

C/C 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:30061737)
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:30061737)
T/T 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:30061737)

Source: GWAS Catalog, Nat Genet 2018, PMID:30061737

Share:

← See all variants