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Who was studied 283,749 European ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.351 lower (95% confidence interval 0.26-0.44); p = 2 × 10−13.
Where it sits Chromosome 9, band 9q21.13 — between genes, 36.8 kb from PCSK5.
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 rs80031788
What is rs80031788?
rs80031788 is a single position in the genome, in or near the near PCSK5 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 rs80031788 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 rs80031788 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 rs80031788 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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