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Who was studied 405,540 European ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.0226 lower (95% confidence interval 0.019-0.026); p = 8 × 10−40.
How common The A allele had a frequency of about 84% in the people studied.
Where it sits Chromosome 14, band 14q11.2 — in an intron of BCL2L2-PABPN1.
What each result means
A/ATwo copies of the version the research linked to Height (baseline). 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 Height (baseline). That is a smaller link than two copies.
G/GNo copy of the version the research linked to Height (baseline). This is the starting point the study compared everyone against.
Nature communications · 2025 · PMID 40374629 · open access
Questions about rs34074573
What is rs34074573?
rs34074573 is a single position in the genome, in or near the BCL2L2-PABPN1 gene. Published research associates it with height (baseline). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs34074573 linked to?
On MyGeneLog this position is linked to Height. The research behind each link, and its sources, are set out on that condition page.
Does having rs34074573 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 rs34074573 come from?
GWAS Catalog, Nature communications 2025, PMID:40374629. 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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