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Who was studied 283,749 European ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.102 lower (95% confidence interval 0.068-0.136); p = 3 × 10−9.
Where it sits Chromosome 20, band 20p12.1 — between genes, 45.6 kb from BANF2.
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 rs2618630
What is rs2618630?
rs2618630 is a single position in the genome, in or near the near BANF2 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 rs2618630 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 rs2618630 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 rs2618630 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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