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FCRLB protein levels

ATF6 · rs80123142

Where this position leads

Condition: Celiac Disease

rs80123142 Condition: Celiac Disease Celiac Disease Condition rs80123142 rs80123142 ATF6

What the study found

Who was studied 47,745 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.569 lower (95% confidence interval 0.5-0.64); p = 1 × 10−66.

How common The A allele had a frequency of about 1% in the people studied.

Where it sits Chromosome 1, band 1q23.3 — in an intron of ATF6.

What each result means

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

Questions about rs80123142

What is rs80123142?

rs80123142 is a single position in the genome, in or near the ATF6 gene. Published research associates it with fcrlb 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 rs80123142 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 rs80123142 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 rs80123142 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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FCRLB protein levels (rs80123142). MyGeneLog™. https://www.mygenelog.com/variants/rs80123142

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