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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 2,599 European ancestry cases, 552,343 European ancestry controls.
The effect
Each copy of the C allele carried 1.80 times the odds of Microscopic colitis (95% confidence interval 1.7-2.0); p = 4 × 10−39.
How common The C allele had a frequency of about 12% in the people studied.
Where it sits Chromosome 6, band 6p21.33 — between genes, 3.8 kb from PPIAP9.
What each result means
C/CTwo copies of the version the research linked to Microscopic colitis. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/GOne copy of the version the research linked to Microscopic colitis. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Microscopic colitis. This is the starting point the study compared everyone against.
Journal of Crohn's & colitis · 2024 · PMID 37768647
Questions about rs9267445
What is rs9267445?
rs9267445 is a single position in the genome, in or near the near PPIAP9 gene. Published research associates it with microscopic colitis. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs9267445 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 rs9267445 come from?
GWAS Catalog, Journal of Crohn's & colitis 2024, PMID:37768647. 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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