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Who was studied 394,642 European ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.0173 higher (95% confidence interval 0.014-0.02); p = 4 × 10−35.
How common The T allele had a frequency of about 55% in the people studied.
Where it sits Chromosome 8, band 8p23.1 — in an intron of XKR6.
What each result means
C/CNo 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.
C/TOne copy of the version the research linked to Impedance of whole body (UKB data field 23106). That is a smaller link than two copies.
T/TTwo 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.
Nature genetics · 2025 · PMID 39789286 · open access
Questions about rs11777007
What is rs11777007?
rs11777007 is a single position in the genome, in or near the XKR6 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 rs11777007 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 rs11777007 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 rs11777007 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) (rs11777007). MyGeneLog™. https://www.mygenelog.com/variants/rs11777007