Who was studied 253,288 European ancestry individuals; replicated in 80,067 European ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.027 higher (95% confidence interval 0.021-0.033); p = 2 × 10−20.
How common The A allele had a frequency of about 57% in the people studied.
Where it sits Chromosome 1, band 1p36.12 — between genes, 0.1 kb from LUZP1.
What each result means
A/APublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Height compared to the general population.
A/GPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Height.
G/GPublished research associates this genotype with typical/baseline likelihood of Height — no copies of the reported risk allele.
Nature genetics · 2014 · PMID 25282103 · open access
Questions about rs2806561
What is rs2806561?
rs2806561 is a single position in the genome, in or near the LUZP1 gene. Published research associates it with height. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs2806561 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 rs2806561 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 rs2806561 come from?
GWAS Catalog, Nature genetics 2014, PMID:25282103. 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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