Standard

Atrial fibrillation

OPN1SW · rs55985730

Share:

Where this position leads

Condition: Atrial Fibrillation (PITX2 Genetic Risk)

rs55985730 Condition: Atrial Fibrillation (PITX2 Genetic Risk) Atrial Fibrillation (PITX2 Genetic Risk) Condition rs55985730 OPN1SW

What each result means

G/G 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)
G/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