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Who was studied 5,314,291 European ancestry, Hispanic or Latin American, East Asian ancestry, African ancestry, South Asian ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.0279 lower (95% confidence interval 0.02-0.036); p = 4 × 10−11.
How common The A allele had a frequency of about 2% in the people studied.
Where it sits Chromosome 16, band 16p13.3 — in an intron of PDPK1.
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.
rs13336495 is a single position in the genome, in or near the PDPK1 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 rs13336495 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 rs13336495 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 rs13336495 come from?
GWAS Catalog, Nature 2022, PMID:36224396. 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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