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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 10,846 European ancestry cases, 11,672 European ancestry controls.
The effect
Each copy of the T allele shifted the measure 0.23 higher (95% confidence interval 0.17-0.29); p = 1 × 10−14.
How common The T allele had a frequency of about 13% in the people studied.
Where it sits Chromosome 1, band 1p12 — in an intron of WARS2.
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 · 2017 · PMID 28272467 · open access
Questions about rs17185996
What is rs17185996?
rs17185996 is a single position in the genome, in or near the WARS2 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 rs17185996 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 rs17185996 come from?
GWAS Catalog, Nature communications 2017, PMID:28272467. 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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