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Glycated hemoglobin levels

MFSD2B · rs3731620

What the study found

Who was studied 327,177 European ancestry individuals, 4,847 African ancestry individuals, 6,895 South Asian ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.0274 lower (95% confidence interval 0.021-0.034); p = 4 × 10−15.

Where it sits Chromosome 2, band 2p23.3 — a missense change in MFSD2B.

What each result means

A/A Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Glycated hemoglobin 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 Glycated hemoglobin levels.
G/G Published research associates this genotype with typical/baseline likelihood of Glycated hemoglobin levels — no copies of the reported risk allele.
Source

Questions about rs3731620

What is rs3731620?

rs3731620 is a single position in the genome, in or near the MFSD2B gene. Published research associates it with glycated hemoglobin levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs3731620 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 rs3731620 come from?

GWAS Catalog, Nature genetics 2021, PMID:33462484. 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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Glycated hemoglobin levels (rs3731620). MyGeneLog™. https://www.mygenelog.com/variants/rs3731620

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