Standard

Incident atrial fibrillation

NEURL1 · rs60848348

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Where this position leads

Condition: Atrial Fibrillation (PITX2 Genetic Risk)

rs60848348 Condition: Atrial Fibrillation (PITX2 Genetic Risk) Atrial Fibrillation (PITX2 Genetic Risk) Condition rs60848348 NEURL1

What each result means

C/C Published research associates this genotype with typical/baseline likelihood of Incident atrial fibrillation — no copies of the reported risk allele. (GWAS Catalog, Nat Genet 2017, PMID:28416818)
C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Incident atrial fibrillation. (GWAS Catalog, Nat Genet 2017, PMID:28416818)
T/T Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Incident atrial fibrillation compared to the general population. (GWAS Catalog, Nat Genet 2017, PMID:28416818)

Source: GWAS Catalog, Nat Genet 2017, PMID:28416818

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