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Who was studied 405,540 European ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.0242 lower (95% confidence interval 0.017-0.031); p = 4 × 10−11.
How common The C allele had a frequency of about 97% in the people studied.
Where it sits Chromosome 4, band 4q31.21 — between genes, 27.5 kb from LINC02266.
What each result means
C/CPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Height (baseline) compared to the general population.
C/GPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Height (baseline).
G/GPublished research associates this genotype with typical/baseline likelihood of Height (baseline) — no copies of the reported risk allele.
Nature communications · 2025 · PMID 40374629 · open access
Questions about rs113854831
What is rs113854831?
rs113854831 is a single position in the genome, in or near the near LINC02266 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 rs113854831 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 rs113854831 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 rs113854831 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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