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CPA4 protein levels

AHCYL2 · rs75009960

Where this position leads

Condition: Celiac Disease

Drug: Fenofibrate

rs75009960 Condition: Celiac Disease Celiac Disease Condition Drug: Fenofibrate Fenofibrate Drug rs75009960 rs75009960 AHCYL2

What the study found

Who was studied 47,745 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.101 higher (95% confidence interval 0.076-0.126); p = 2 × 10−17.

How common The T allele had a frequency of about 5% in the people studied.

Where it sits Chromosome 7, band 7q32.1 — in an intron of AHCYL2.

What each result means

A/A No copy of the version the research linked to CPA4 protein levels. This is the starting point the study compared everyone against.
A/T One copy of the version the research linked to CPA4 protein levels. That is a smaller link than two copies.
T/T Two copies of the version the research linked to CPA4 protein levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs75009960

What is rs75009960?

rs75009960 is a single position in the genome, in or near the AHCYL2 gene. Published research associates it with cpa4 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 rs75009960 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 rs75009960 affect how medicines work?

AHCYL2 carries pharmacogenomic findings for Fenofibrate. That is educational information, not a prescription or a dosing guide. Any decision to start, stop or change a medicine belongs with the clinician or pharmacist managing your treatment.

Does having rs75009960 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 rs75009960 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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CPA4 protein levels (rs75009960). MyGeneLog™. https://www.mygenelog.com/variants/rs75009960

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