Sensitive

Inflammatory bowel disease

CEBPB · rs913678

Where this position leads

Condition: Inflammatory Bowel Disease

rs913678 Condition: Inflammatory Bowel Disease Inflammatory Bowel Disease Condition rs913678 rs913678 CEBPB

What the study found

Who was studied 12,924 European ancestry cases, 21,442 European ancestry controls; replicated in 25,683 European ancestry cases, 17,015 European ancestry controls.

The effect Each copy of the T allele carried 1.06 times the odds of Inflammatory bowel disease (95% confidence interval 1.024-1.088); p = 5 × 10−8.

How common The T allele had a frequency of about 66% in the people studied.

Where it sits Chromosome 20, band 20q13.13 — between genes, 11.8 kb from LOC105372657.

What each result means

C/C No copy of the version the research linked to Inflammatory bowel disease. This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Inflammatory bowel disease. That is a smaller link than two copies.
T/T Two copies of the version the research linked to Inflammatory bowel disease. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs913678

What is rs913678?

rs913678 is a single position in the genome, in or near the CEBPB gene. Published research associates it with inflammatory bowel disease. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs913678 linked to?

On MyGeneLog this position is linked to Inflammatory Bowel Disease. The research behind each link, and its sources, are set out on that condition page.

Does having rs913678 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 rs913678 come from?

GWAS Catalog, Nature 2012, PMID:23128233. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

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Inflammatory bowel disease (rs913678). MyGeneLog™. https://www.mygenelog.com/variants/rs913678

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