Sensitive

Crohn's disease-related phenotypes

MAGI1 · rs11924265

Where this position leads

Condition: Crohn's Disease

rs11924265 Condition: Crohn's Disease Crohn's Disease Condition rs11924265 rs11924265 MAGI1

What the study found

Who was studied up to 1,090 Southern European ancestry Crohn's disease cases; replicated in up to 1,296 Southern European ancestry Crohn's disease cases.

The effect Each copy of the C allele carried 2.03 times the odds of Crohn's disease-related phenotypes (95% confidence interval 1.52-2.73); p = 5 × 10−7.

How common The C allele had a frequency of about 6% in the people studied.

Where it sits Chromosome 3, band 3p14.1 — in an intron of LOC107986018.

What each result means

C/C Two copies of the version the research linked to Crohn's disease-related phenotypes. 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-related phenotypes. That is a smaller link than two copies.
T/T No copy of the version the research linked to Crohn's disease-related phenotypes. This is the starting point the study compared everyone against.
Source

Questions about rs11924265

What is rs11924265?

rs11924265 is a single position in the genome, in or near the MAGI1 gene. Published research associates it with crohn's disease-related phenotypes. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs11924265 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 rs11924265 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 rs11924265 come from?

GWAS Catalog, Gastroenterology 2014, PMID:25557950. 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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Crohn's disease-related phenotypes (rs11924265). MyGeneLog™. https://www.mygenelog.com/variants/rs11924265

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