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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 52,874 British ancestry males.
The effect
Each copy of the A allele shifted the measure 0.332 lower; p = 5 × 10−18.
Where it sits Chromosome X, band Xq12 — between genes, 14.3 kb from MIR223HG.
What each result means
A/ATwo 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.
A/GOne copy of the version the research linked to Male-pattern baldness. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Male-pattern baldness. This is the starting point the study compared everyone against.
PLoS genetics · 2017 · PMID 28196072 · open access
Questions about rs73213393
What is rs73213393?
rs73213393 is a single position in the genome, in or near the near MIR223HG 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.
Does having rs73213393 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 rs73213393 come from?
GWAS Catalog, PLoS genetics 2017, PMID:28196072. 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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