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Who was studied 283,749 European ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.157 lower (95% confidence interval 0.1-0.21); p = 4 × 10−9.
Where it sits Chromosome 12, band 12q23.3 — between genes, 5.2 kb from EEF1B2P4.
What each result means
C/CTwo copies of the version the research linked to Height (standard GWA). That is the strongest link of the three results. A link in a study is not a diagnosis.
C/TOne copy of the version the research linked to Height (standard GWA). That is a smaller link than two copies.
T/TNo copy of the version the research linked to Height (standard GWA). This is the starting point the study compared everyone against.
Nature human behaviour · 2023 · PMID 37106081 · open access
Questions about rs11113137
What is rs11113137?
rs11113137 is a single position in the genome, in or near the near EEF1B2P4 gene. Published research associates it with height (standard gwa). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs11113137 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 rs11113137 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 rs11113137 come from?
GWAS Catalog, Nature human behaviour 2023, PMID:37106081. 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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