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Gamma glutamyl transferase levels

DYNLRB2-AS1 · rs4581712

What the study found

Who was studied 507,850 East Asian ancestry individuals, 420,829 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.0379 higher (95% confidence interval 0.035-0.041); p = 6 × 10−121.

Where it sits Chromosome 16, band 16q23.2 — in an intron of DYNLRB2-AS1.

What each result means

A/A Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Gamma glutamyl transferase levels compared to the general population.
A/C Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Gamma glutamyl transferase levels.
C/C Published research associates this genotype with typical/baseline likelihood of Gamma glutamyl transferase levels — no copies of the reported risk allele.
Source

Questions about rs4581712

What is rs4581712?

rs4581712 is a single position in the genome, in or near the DYNLRB2-AS1 gene. Published research associates it with gamma glutamyl transferase levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs4581712 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 rs4581712 come from?

GWAS Catalog, Nature communications 2025, PMID:40436827. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

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Gamma glutamyl transferase levels (rs4581712). MyGeneLog™. https://www.mygenelog.com/variants/rs4581712

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