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The effect
Each copy of the T allele shifted the measure 0.169 lower (95% confidence interval 0.15-0.19); p = 9 × 10−99.
How common The T allele had a frequency of about 4% in the people studied.
Where it sits Chromosome 2, band 2p23.1 — between genes, 104 kb from LINC01946.
What each result means
C/CNo copy of the version the research linked to Male-pattern baldness. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Male-pattern baldness. That is a smaller link than two copies.
T/TTwo 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 rs76712439
What is rs76712439?
rs76712439 is a single position in the genome, in or near the near SRD5A2 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 rs76712439 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 rs76712439 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 rs76712439 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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