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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 7,049 European ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.09 lower (95% confidence interval 0.07-0.11); p = 7 × 10−10.
How common The A allele had a frequency of about 69% in the people studied.
Where it sits Chromosome 2, band 2q22.3 — in an intron of TEX41.
What each result means
A/ATwo copies of the version the research linked to Anti-Mullerian hormone 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 Anti-Mullerian hormone levels. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Anti-Mullerian hormone levels. This is the starting point the study compared everyone against.
Human reproduction (Oxford, England) · 2022 · PMID 35274129 · open access
Questions about rs13009019
What is rs13009019?
rs13009019 is a single position in the genome, in or near the TEX41 gene. Published research associates it with anti-mullerian hormone levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs13009019 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 rs13009019 come from?
GWAS Catalog, Human reproduction (Oxford, England) 2022, PMID:35274129. 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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