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GGH protein levels

CYP7B1 · rs536808557

Where this position leads

Condition: Celiac Disease

rs536808557 Condition: Celiac Disease Celiac Disease Condition rs536808557 rs536808557 CYP7B1

What the study found

Who was studied 47,745 European ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.319 higher (95% confidence interval 0.22-0.42); p = 2 × 10−11.

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

Where it sits Chromosome 8, band 8q12.3 — in an intron of CYP7B1.

What each result means

A/A No copy of the version the research linked to GGH protein levels. This is the starting point the study compared everyone against.
A/G One copy of the version the research linked to GGH protein levels. That is a smaller link than two copies.
G/G 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.
Source

Questions about rs536808557

What is rs536808557?

rs536808557 is a single position in the genome, in or near the CYP7B1 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 rs536808557 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 rs536808557 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 rs536808557 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 (rs536808557). MyGeneLog™. https://www.mygenelog.com/variants/rs536808557

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