rs57062879 CDC123
A allele associated with marginally increased risk of Chronic obstructive pulmonary disease x current smoker interaction (main effect) (OR=1.11). [GWAS Catalog]
What is rs57062879?
rs57062879 is a single-nucleotide polymorphism (SNP) in the CDC123 gene. Each person carries two copies, one from each parent, so a result is reported as a pair of letters such as AA. The table below describes what studies associate with each genotype; the association is statistical, across populations, and is not a diagnosis.
What does each rs57062879 genotype mean?
| Genotype | Association | What the evidence says | Confidence |
|---|---|---|---|
| AA | typical | A allele associated with marginally increased risk of Chronic obstructive pulmonary disease x current smoker interaction (main effect) (OR=1.11). [GWAS Catalog] | 75% |
Is rs57062879 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
- PubMed 33106845
- GWAS Catalog
- GCST90016591
Upload your 23andMe, AncestryDNA or WeGene raw file → · Ask G2: “What is my genotype at rs57062879 and what does it mean for me?”
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.