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Glycated hemoglobin levels

SCRN3 · rs17256082

What the study found

Who was studied 146,806 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.0069 higher; p = 3 × 10−8.

How common The T allele had a frequency of about 67% in the people studied.

Where it sits Chromosome 2, band 2q31.1 — in an intron of SCRN3.

What each result means

C/C No copy of the version the research linked to Glycated hemoglobin levels. This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Glycated hemoglobin levels. That is a smaller link than two copies.
T/T Two copies of the version the research linked to Glycated hemoglobin levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs17256082

What is rs17256082?

rs17256082 is a single position in the genome, in or near the SCRN3 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 rs17256082 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 rs17256082 come from?

GWAS Catalog, Nature genetics 2021, PMID:34059833. 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 (rs17256082). MyGeneLog™. https://www.mygenelog.com/variants/rs17256082

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