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Gamma glutamyl transpeptidase

near BHLHA15 · rs140409516

What the study found

Who was studied 344,104 European ancestry individuals, 133,471 East Asian ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.0277 higher (95% confidence interval 0.021-0.035); p = 4 × 10−15.

Where it sits Chromosome 7, band 7q21.3 — between genes, 0 kb from BHLHA15.

What each result means

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

Questions about rs140409516

What is rs140409516?

rs140409516 is a single position in the genome, in or near the near BHLHA15 gene. Published research associates it with gamma glutamyl transpeptidase. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs140409516 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 rs140409516 come from?

GWAS Catalog, Nature genetics 2021, PMID:34594039. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.

Gamma glutamyl transpeptidase (rs140409516). MyGeneLog™. https://www.mygenelog.com/variants/rs140409516

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