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The effect
Each copy of the C allele shifted the measure 0.0182 higher (95% confidence interval 0.012-0.025); p = 1 × 10−8.
How common The C allele had a frequency of about 36% in the people studied.
Where it sits Chromosome 8, band 8p12 — between genes, 32.1 kb from MAP2K1P1.
What each result means
C/CTwo 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.
C/TOne copy of the version the research linked to Male-pattern baldness. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Male-pattern baldness. This is the starting point the study compared everyone against.
Nature communications · 2018 · PMID 30573740 · open access
Questions about rs2595041
What is rs2595041?
rs2595041 is a single position in the genome, in or near the near SARAF 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 rs2595041 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 rs2595041 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 rs2595041 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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