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Who was studied 405,540 European ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.0121 higher (95% confidence interval 0.0095-0.0147); p = 1 × 10−19.
How common The T allele had a frequency of about 63% in the people studied.
Where it sits Chromosome 11, band 11q24.2 — between genes, 43.1 kb from NAP1L1P1.
What each result means
C/CNo copy of the version the research linked to Height (baseline). This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Height (baseline). That is a smaller link than two copies.
T/TTwo 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.
Nature communications · 2025 · PMID 40374629 · open access
Questions about rs511987
What is rs511987?
rs511987 is a single position in the genome, in or near the near NAP1L1P1 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 rs511987 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 rs511987 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 rs511987 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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