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CST7 protein levels

EFCAB8 · rs565584800

Where this position leads

Condition: Celiac Disease

rs565584800 Condition: Celiac Disease Celiac Disease Condition rs565584800 rs565584800 EFCAB8

What the study found

Who was studied 47,745 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.544 higher (95% confidence interval 0.37-0.72); p = 1 × 10−12.

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

Where it sits Chromosome 20, band 20q11.21 — in an intron of EFCAB8.

What each result means

A/A Two copies of the version the research linked to CST7 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 CST7 protein levels. That is a smaller link than two copies.
G/G No copy of the version the research linked to CST7 protein levels. This is the starting point the study compared everyone against.
Source

Questions about rs565584800

What is rs565584800?

rs565584800 is a single position in the genome, in or near the EFCAB8 gene. Published research associates it with cst7 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 rs565584800 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 rs565584800 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 rs565584800 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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CST7 protein levels (rs565584800). MyGeneLog™. https://www.mygenelog.com/variants/rs565584800

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