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Who was studied 394,642 European ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.012 higher (95% confidence interval 0.0085-0.0154); p = 6 × 10−13.
How common The A allele had a frequency of about 77% in the people studied.
Where it sits Chromosome 7, band 7p14.1 — in an intron of POU6F2.
What each result means
A/ATwo copies of the version the research linked to Impedance of whole body (UKB data field 23106). That is the strongest link of the three results. A link in a study is not a diagnosis.
A/GOne copy of the version the research linked to Impedance of whole body (UKB data field 23106). That is a smaller link than two copies.
G/GNo copy of the version the research linked to Impedance of whole body (UKB data field 23106). This is the starting point the study compared everyone against.
Nature genetics · 2025 · PMID 39789286 · open access
Questions about rs4629764
What is rs4629764?
rs4629764 is a single position in the genome, in or near the POU6F2 gene. Published research associates it with impedance of whole body (ukb data field 23106). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs4629764 linked to?
On MyGeneLog this position is linked to Celiac Disease. The research behind each link, and its sources, are set out on that condition page.
Does having rs4629764 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 rs4629764 come from?
GWAS Catalog, Nature genetics 2025, PMID:39789286. 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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Quoting this page
Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.
Impedance of whole body (UKB data field 23106) (rs4629764). MyGeneLog™. https://www.mygenelog.com/variants/rs4629764