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HMOX2 protein levels

CORO7-PAM16 · rs140044442

Where this position leads

Condition: Celiac Disease

rs140044442 Condition: Celiac Disease Celiac Disease Condition rs140044442 rs140044442 CORO7-PAM16

What the study found

Who was studied 47,745 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.448 higher (95% confidence interval 0.31-0.58); p = 7 × 10−12.

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

Where it sits Chromosome 16, band 16p13.3 — inside CORO7-PAM16.

What each result means

A/A No copy of the version the research linked to HMOX2 protein levels. This is the starting point the study compared everyone against.
A/T One copy of the version the research linked to HMOX2 protein levels. That is a smaller link than two copies.
T/T Two copies of the version the research linked to HMOX2 protein levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs140044442

What is rs140044442?

rs140044442 is a single position in the genome, in or near the CORO7-PAM16 gene. Published research associates it with hmox2 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 rs140044442 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 rs140044442 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 rs140044442 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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HMOX2 protein levels (rs140044442). MyGeneLog™. https://www.mygenelog.com/variants/rs140044442

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