CRY2 · rs12794698
Where this position leads
Condition: Fasting Blood Glucose
What the study found
Who was studied 153,950 Korean ancestry individuals.
The effect Each copy of the A allele shifted the measure 0.0337 lower (95% confidence interval 0.025-0.042); p = 4 × 10−15.
How common The A allele had a frequency of about 21% in the people studied.
Where it sits Chromosome 11, band 11p11.2 — in an intron of CRY2.
rs12794698 is a single position in the genome, in or near the CRY2 gene. Published research associates it with fasting blood glucose. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
On MyGeneLog this position is linked to Fasting Blood Glucose. The research behind each link, and its sources, are set out on that condition page.
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.
GWAS Catalog, Nature communications 2025, PMID:40436827. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
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.
Fasting blood glucose (rs12794698). MyGeneLog™. https://www.mygenelog.com/variants/rs12794698