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Serum metabolite levels

AGXT2 · rs37371

What the study found

Who was studied 3,926 Hispanic/Latino individuals.

The effect Each copy of the A allele shifted the measure 0.302 higher (95% confidence interval 0.25-0.36); p = 2 × 10−26.

How common The A allele had a frequency of about 22% in the people studied.

Where it sits Chromosome 5, band 5p13.2 — in an intron of AGXT2.

What each result means

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

Questions about rs37371

What is rs37371?

rs37371 is a single position in the genome, in or near the AGXT2 gene. Published research associates it with serum metabolite levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs37371 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 rs37371 come from?

GWAS Catalog, Am J Hum Genet 2020, PMID:33031748. 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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Serum metabolite levels (rs37371). MyGeneLog™. https://www.mygenelog.com/variants/rs37371

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