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ZP3 protein levels

TMEM120A · rs562397873

Where this position leads

Condition: Celiac Disease

rs562397873 Condition: Celiac Disease Celiac Disease Condition rs562397873 rs562397873 TMEM120A

What the study found

Who was studied 47,745 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.297 lower (95% confidence interval 0.18-0.42); p = 3 × 10−12.

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

Where it sits Chromosome 7, band 7q11.23 — in an intron of TMEM120A.

What each result means

A/A Two copies of the version the research linked to ZP3 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 ZP3 protein levels. That is a smaller link than two copies.
G/G No copy of the version the research linked to ZP3 protein levels. This is the starting point the study compared everyone against.
Source

Questions about rs562397873

What is rs562397873?

rs562397873 is a single position in the genome, in or near the TMEM120A gene. Published research associates it with zp3 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 rs562397873 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 rs562397873 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 rs562397873 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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ZP3 protein levels (rs562397873). MyGeneLog™. https://www.mygenelog.com/variants/rs562397873

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