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APOD protein levels

near MLXIPL · rs7786376

Where this position leads

Condition: Celiac Disease

rs7786376 Condition: Celiac Disease Celiac Disease Condition rs7786376 rs7786376 near MLXIPL

What the study found

Who was studied 47,745 European ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.0428 higher (95% confidence interval 0.03-0.055); p = 9 × 10−13.

How common The G allele had a frequency of about 28% in the people studied.

Where it sits Chromosome 7, band 7q11.23 — between genes, 3.7 kb from MLXIPL.

What each result means

A/A No copy of the version the research linked to APOD protein levels. This is the starting point the study compared everyone against.
A/G One copy of the version the research linked to APOD protein levels. That is a smaller link than two copies.
G/G Two copies of the version the research linked to APOD protein levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs7786376

What is rs7786376?

rs7786376 is a single position in the genome, in or near the near MLXIPL gene. Published research associates it with apod protein levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs7786376 linked to?

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

Does having rs7786376 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 rs7786376 come from?

GWAS Catalog, Nature genetics 2025, PMID:39789286. 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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APOD protein levels (rs7786376). MyGeneLog™. https://www.mygenelog.com/variants/rs7786376

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