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Glycated hemoglobin levels

near GPR161 · rs78343926

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 T allele shifted the measure 0.0378 higher (95% confidence interval 0.026-0.049); p = 2 × 10−10.

Where it sits Chromosome 1, band 1q24.2 — between genes, 6.8 kb from GPR161.

What each result means

C/C Published research associates this genotype with typical/baseline likelihood of Glycated hemoglobin 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 Glycated hemoglobin levels.
T/T 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.
Source

Questions about rs78343926

What is rs78343926?

rs78343926 is a single position in the genome, in or near the near GPR161 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 rs78343926 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 rs78343926 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

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.

Glycated hemoglobin levels (rs78343926). MyGeneLog™. https://www.mygenelog.com/variants/rs78343926

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