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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.
Strength of the evidence
2 / 4
Its strongest genetic-study result is p = 10−22, with 3 associations in the GWAS Catalog.
How this is scored
4: ClinVar disease-causing, reviewed by an expert panel or a guideline (3–4 stars). 3: ClinVar, several labs agreeing (2 stars), or a genetic study at p ≤ 10−50. 2: ClinVar from one lab (1 star), or p ≤ 10−20. 1: ClinVar submitted without criteria (0 stars), or genome-wide significance (p ≤ 5×10−8). The higher of the two counts. It says how solid the evidence is, not whether it matters for a particular person.
What the study found
Who was studied 235,579 European ancestry females.
The effect
Each copy of the A allele shifted the measure 0.0426 higher (95% confidence interval 0.034-0.051); p = 3 × 10−22.
How common The A allele had a frequency of about 13% in the people studied.
Where it sits Chromosome 7, band 7q11.23 — between genes, 10.3 kb from MLXIPL.
What each result means
A/ATwo 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.
A/GOne copy of the version the research linked to Testosterone levels. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Testosterone levels. This is the starting point the study compared everyone against.
Nature genetics · 2025 · PMID 40229599 · open access
Questions about rs13234805
What is rs13234805?
rs13234805 is a single position in the genome, in or near the near MLXIPL 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 rs13234805 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 rs13234805 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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