Sensitive

Esophageal cancer

ACAD10 · rs11066015

Stands on its own. Nothing else here links to this position yet — but the page above is the point: what the research found, what each genotype means, and where it came from, in language you can read. Links to conditions, drugs and the senses appear automatically if we write them.

What each result means

A/A Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Esophageal cancer compared to the general population. (GWAS Catalog, Nat Genet 2011, PMID:21642993)

A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Esophageal cancer. (GWAS Catalog, Nat Genet 2011, PMID:21642993)

G/G Published research associates this genotype with typical/baseline likelihood of Esophageal cancer — no copies of the reported risk allele. (GWAS Catalog, Nat Genet 2011, PMID:21642993)

Source: GWAS Catalog, Nat Genet 2011, PMID:21642993

Questions about rs11066015

What is rs11066015?

rs11066015 is a single position in the genome, in or near the ACAD10 gene. Published research associates it with esophageal cancer. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs11066015 mean I will get this?

No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.

Where does the information about rs11066015 come from?

GWAS Catalog, Nat Genet 2011, PMID:21642993. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

← See all variants