Sensitive

Crohn's disease

AKAP11 · rs80244186

Where this position leads

Condition: Crohn's Disease

rs80244186 Condition: Crohn's Disease Crohn's Disease Condition rs80244186 rs80244186 AKAP11

What the study found

Who was studied 12,194 European and unknown ancestry cases, 28,072 European and unknown ancestry controls.

The effect Each copy of the C allele carried 1.13 times the odds of Crohn's disease (95% confidence interval 1.09–1.18); p = 4 × 10−8.

How common The C allele had a frequency of about 11% in the people studied.

Where it sits Chromosome 13, band 13q14.11 — in an intron of LINC02341.

What each result means

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

Questions about rs80244186

What is rs80244186?

rs80244186 is a single position in the genome, in or near the AKAP11 gene. Published research associates it with crohn's 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 rs80244186 linked to?

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

Does having rs80244186 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 rs80244186 come from?

GWAS Catalog, Nat Genet 2017, PMID:28067908. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

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.

Crohn's disease (rs80244186). MyGeneLog™. https://www.mygenelog.com/variants/rs80244186

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