Standard

Atrial fibrillation

LRIG1 · rs2306272

Share:

Where this position leads

Condition: Atrial Fibrillation (PITX2 Genetic Risk)

rs2306272 Condition: Atrial Fibrillation (PITX2 Genetic Risk) Atrial Fibrillation (PITX2 Genetic Risk) Condition rs2306272 LRIG1

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: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 with typical/baseline likelihood of Atrial fibrillation — no copies of the reported risk allele. (GWAS Catalog, Nat Genet 2018, PMID:29892015)

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

Share:

← See all variants