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The effect
Each copy of the A allele shifted the measure 0.0227 lower (95% confidence interval 0.016-0.03); p = 3 × 10−10.
How common The A allele had a frequency of about 24% in the people studied.
Where it sits Chromosome 2, band 2p14 — inside LINC01798.
What each result means
A/APublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Male-pattern baldness compared to the general population.
A/CPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Male-pattern baldness.
C/CPublished research associates this genotype with typical/baseline likelihood of Male-pattern baldness — no copies of the reported risk allele.
Nature communications · 2018 · PMID 30573740 · open access
Questions about rs10206999
What is rs10206999?
rs10206999 is a single position in the genome, in or near the near MEIS1 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 rs10206999 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 rs10206999 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 rs10206999 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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