Orviva

Learn · Variants · EED

rs6592278 EED

C allele associated with increased Smoking initiation (β=0.008). [GWAS Catalog]

Imported from public databases · not individually reviewed Trait · Risk / effect allele: C · dbSNP

What is rs6592278?

rs6592278 is a single-nucleotide polymorphism (SNP) in the EED gene. Each person carries two copies, one from each parent, so a result is reported as a pair of letters such as CC. The table below describes what studies associate with each genotype; the association is statistical, across populations, and is not a diagnosis.

What does each rs6592278 genotype mean?

GenotypeAssociationWhat the evidence saysConfidence
CCincreasedC allele associated with increased Smoking initiation (β=0.008). [GWAS Catalog]75%

Is rs6592278 on 23andMe and AncestryDNA chips?

Chip coverage is not recorded for this variant. Orviva reports it when a raw-data file contains it directly or via a well-correlated proxy SNP, and says so when it does not.

Sources

Genetic associations describe risk across populations, not a diagnosis for any one person. Most variants shift risk modestly and act alongside lifestyle, environment and other genes. Consumer DNA chips do not read every position and can be wrong at any single one. For general education only; talk to a clinician or genetic counsellor before acting on anything here, and never change a prescribed medicine without your prescriber.