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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 T allele shifted the measure 0.286 higher (95% confidence interval 0.19-0.38); p = 2 × 10−9.
How common The T allele had a frequency of about 2% in the people studied.
Where it sits Chromosome 3, band 3p22.1 — in an intron of TRAK1.
What each result means
C/CNo copy of the version the research linked to CAG-884 abundance in stool. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to CAG-884 abundance in stool. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to CAG-884 abundance in stool. That is the strongest link of the three results. A link in a study is not a diagnosis.
rs76416179 is a single position in the genome, in or near the TRAK1 gene. Published research associates it with cag-884 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 rs76416179 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 rs76416179 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-884 abundance in stool (rs76416179). MyGeneLog™. https://www.mygenelog.com/variants/rs76416179