Sensitive

Breast cancer

near MRPS30 · rs10941679

Where this position leads

Condition: Breast Cancer

rs10941679 Condition: Breast Cancer Breast Cancer Condition Topic: Menopause Menopause Topic Topic: Fertility Fertility Topic rs10941679 rs10941679 near MRPS30

Solid lines are connections this site curates. Dashed lines mean the two ends share a research paper — worth knowing, and not a claim that one explains the other.

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

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 rs10941679

What is rs10941679?

rs10941679 is a single position in the genome, in or near the near MRPS30 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 rs10941679 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 rs10941679?

Subjects that appear in the title or abstract of the same papers as this rsID include menopause (5 papers), fertility (3 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.

Does having rs10941679 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 rs10941679 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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