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GGH protein levels

GGH · rs182166268

Where this position leads

Condition: Celiac Disease

rs182166268 Condition: Celiac Disease Celiac Disease Condition rs182166268 rs182166268 GGH

What the study found

Who was studied 47,745 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.353 lower (95% confidence interval 0.24-0.46); p = 1 × 10−11.

How common The A allele had a frequency of about 0% in the people studied.

Where it sits Chromosome 8, band 8q12.3 — in an intron of GGH.

What each result means

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

Questions about rs182166268

What is rs182166268?

rs182166268 is a single position in the genome, in or near the GGH gene. Published research associates it with ggh 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 rs182166268 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 rs182166268 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 rs182166268 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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GGH protein levels (rs182166268). MyGeneLog™. https://www.mygenelog.com/variants/rs182166268

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