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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 887,490 European ancestry individuals (MTAG effective sample size boosted by neuroticism, depression and anxiety samples).
The effect
Each copy of the T allele shifted the measure 0.01 lower (95% confidence interval 0.0061-0.0139); p = 1 × 10−9.
Where it sits Chromosome 13, band 13q21.1 — between genes, 78.6 kb from CTAGE16P.
What each result means
G/GNo copy of the version the research linked to Irritable bowel syndrome (MTAG). This is the starting point the study compared everyone against.
G/TOne copy of the version the research linked to Irritable bowel syndrome (MTAG). That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Irritable bowel syndrome (MTAG). That is the strongest link of the three results. A link in a study is not a diagnosis.
Journal of translational medicine · 2023 · PMID 37085903 · open access
Questions about rs9597797
What is rs9597797?
rs9597797 is a single position in the genome, in or near the near CTAGE16P gene. Published research associates it with irritable bowel syndrome (mtag). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs9597797 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 rs9597797 come from?
GWAS Catalog, Journal of translational medicine 2023, PMID:37085903. 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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