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Glycated hemoglobin levels

TSPAN15 · rs7090788

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 0.0418 lower (95% confidence interval 0.033-0.051); p = 2 × 10−20.

Where it sits Chromosome 10, band 10q22.1 — in an intron of TSPAN15.

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

Questions about rs7090788

What is rs7090788?

rs7090788 is a single position in the genome, in or near the TSPAN15 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 rs7090788 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 rs7090788 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 (rs7090788). MyGeneLog™. https://www.mygenelog.com/variants/rs7090788

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