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Stands on its own.
Nothing else here links to this position yet — but the page above is the point: what the
research found, what each genotype means, and where it came from, in language you can
read. Links to conditions, drugs and the senses appear automatically if we write them.
What the study found
Who was studied 5,959 Finnish ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.185 higher (95% confidence interval 0.12-0.25); p = 4 × 10−9.
How common The C allele had a frequency of about 5% in the people studied.
Where it sits Chromosome 10, band 10q22.1 — in an intron of ANAPC16.
What each result means
C/CTwo copies of the version the research linked to CAG-776 abundance in stool. 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 CAG-776 abundance in stool. That is a smaller link than two copies.
T/TNo copy of the version the research linked to CAG-776 abundance in stool. This is the starting point the study compared everyone against.
rs10823909 is a single position in the genome, in or near the ANAPC16 gene. Published research associates it with cag-776 abundance in stool. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs10823909 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 rs10823909 come from?
GWAS Catalog, Nature genetics 2022, PMID:35115689. 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.
CAG-776 abundance in stool (rs10823909). MyGeneLog™. https://www.mygenelog.com/variants/rs10823909