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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 the study found
Who was studied 24,579 European ancestry females.
The effect
Each copy of the G allele shifted the measure 5.53 z score lower; p = 3 × 10−8.
How common The G allele had a frequency of about 47% in the people studied.
Where it sits Chromosome 22, band 22q13.1 — between genes, 0.1 kb from MAFF.
What each result means
A/ANo copy of the version the research linked to Mammographic density (dense area). This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Mammographic density (dense area). That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Mammographic density (dense area). That is the strongest link of the three results. A link in a study is not a diagnosis.
Breast cancer research : BCR · 2022 · PMID 35414113 · open access
Questions about rs34066050
What is rs34066050?
rs34066050 is a single position in the genome, in or near the MAFF gene. Published research associates it with mammographic density (dense area). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs34066050 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 rs34066050 come from?
GWAS Catalog, Breast cancer research : BCR 2022, PMID:35414113. 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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Quoting this page
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Mammographic density (dense area) (rs34066050). MyGeneLog™. https://www.mygenelog.com/variants/rs34066050