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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 246,862 European and South Asian ancestry females.
The effect
Each copy of the G allele shifted the measure 0.0265 lower (95% confidence interval 0.02-0.033); p = 7 × 10−16.
How common The G allele had a frequency of about 26% in the people studied.
Where it sits Chromosome 1, band 1p13.2 — in the 3′ untranslated region of ST7L.
What each result means
A/ANo copy of the version the research linked to Testosterone levels. This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Testosterone levels. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Testosterone levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature genetics · 2025 · PMID 40229599 · open access
Questions about rs3790611
What is rs3790611?
rs3790611 is a single position in the genome, in or near the ST7L gene. Published research associates it with testosterone levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs3790611 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 rs3790611 come from?
GWAS Catalog, Nature genetics 2025, PMID:40229599. 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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