UTC
Sensitive

Breast cancer

COX11 · rs6504950

Where this position leads

Condition: Breast Cancer

rs6504950 Condition: Breast Cancer Breast Cancer Condition rs6504950 rs6504950 COX11

What each result means

A/A Published research associates this genotype with typical/baseline likelihood of Breast cancer — no copies of the reported risk allele. (GWAS Catalog, Nat Genet 2013, PMID:23535729)
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Breast cancer. (GWAS Catalog, Nat Genet 2013, PMID:23535729)
G/G Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Breast cancer compared to the general population. (GWAS Catalog, Nat Genet 2013, PMID:23535729)

Source: GWAS Catalog, Nat Genet 2013, PMID:23535729

What people read about alongside this

Fertility2 Menopause2

Papers in Europe PMC whose title or abstract names both this rsID and that subject. A shared paper means somebody wrote about the two together — it is not a claim that this position explains the subject.

Questions about rs6504950

What is rs6504950?

rs6504950 is a single position in the genome, in or near the COX11 gene. Published research associates it with breast cancer. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs6504950 linked to?

On MyGeneLog this position is linked to Breast Cancer. The research behind each link, and its sources, are set out on that condition page.

What do people read about alongside rs6504950?

Subjects that appear in the title or abstract of the same papers as this rsID include fertility (2 papers), menopause (2 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.

Does having rs6504950 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 rs6504950 come from?

GWAS Catalog, Nat Genet 2013, PMID:23535729. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

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