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Who was studied 153,950 Korean ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.0258 lower (95% confidence interval 0.019-0.033); p = 7 × 10−13.
How common The A allele had a frequency of about 37% in the people studied.
Where it sits Chromosome 1, band 1p34.2 — in an intron of SLC2A1-DT.
What each result means
A/ATwo copies of the version the research linked to Fasting blood glucose. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/TOne copy of the version the research linked to Fasting blood glucose. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Fasting blood glucose. This is the starting point the study compared everyone against.
Nature communications · 2025 · PMID 40436827 · open access
Questions about rs75244136
What is rs75244136?
rs75244136 is a single position in the genome, in or near the SLC2A1-DT 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.
What conditions is rs75244136 linked to?
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.
Does having rs75244136 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 rs75244136 come from?
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.
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