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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 4,301 European ancestry men, 3,358 European ancestry women.
The effect
Each copy of the T allele shifted the measure 0.0637 higher (95% confidence interval 0.044-0.084); p = 4 × 10−10.
How common The T allele had a frequency of about 42% in the people studied.
Where it sits Chromosome 13, band 13q12.11 — between genes, 20.4 kb from FGF9.
What each result means
A/ANo copy of the version the research linked to DHEAS levels. This is the starting point the study compared everyone against.
A/TOne copy of the version the research linked to DHEAS levels. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to DHEAS levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
The Journal of clinical endocrinology and metabolism · 2019 · PMID 31169883
Questions about rs955783
What is rs955783?
rs955783 is a single position in the genome, in or near the near FGF9 gene. Published research associates it with dheas levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs955783 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 rs955783 come from?
GWAS Catalog, The Journal of clinical endocrinology and metabolism 2019, PMID:31169883. 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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