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The effect
Each copy of the G allele shifted the measure 0.0291 lower (95% confidence interval 0.022-0.036); p = 3 × 10−15.
How common The G allele had a frequency of about 23% in the people studied.
Where it sits Chromosome 3, band 3q25.1 — in an intron of MBNL1.
What each result means
A/ANo copy of the version the research linked to Male-pattern baldness. This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Male-pattern baldness. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Male-pattern baldness. That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature communications · 2018 · PMID 30573740 · open access
Questions about rs13093352
What is rs13093352?
rs13093352 is a single position in the genome, in or near the MBNL1 gene. Published research associates it with male-pattern baldness. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs13093352 linked to?
On MyGeneLog this position is linked to Androgenetic Alopecia (Male Pattern Baldness). The research behind each link, and its sources, are set out on that condition page.
Does having rs13093352 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 rs13093352 come from?
GWAS Catalog, Nat Commun 2018, PMID:30573740. 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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