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Serum metabolite levels

CR936677 · rs4949874

What the study found

Who was studied 3,926 Hispanic/Latino individuals.

The effect Each copy of the T allele shifted the measure 0.356 higher (95% confidence interval 0.31-0.41); p = 9 × 10−48.

How common The T allele had a frequency of about 70% in the people studied.

Where it sits Chromosome 1, band 1p31.1 — between genes, 28.2 kb from ACADM.

What each result means

C/C Published research associates this genotype with typical/baseline likelihood of Serum metabolite levels — no copies of the reported risk allele.
C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Serum metabolite levels.
T/T 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.
Source

Questions about rs4949874

What is rs4949874?

rs4949874 is a single position in the genome, in or near the CR936677 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 rs4949874 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 rs4949874 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.

Quoting this page

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Serum metabolite levels (rs4949874). MyGeneLog™. https://www.mygenelog.com/variants/rs4949874

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