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Stands on its own.
Nothing else here links to this position yet — but the page above is the point: what the
research found, what each genotype means, and where it came from, in language you can
read. Links to conditions, drugs and the senses appear automatically if we write them.
What the study found
Who was studied 56,912 Chinese ancestry females; replicated in up to 20,026 East Asian ancestry females.
The effect
Each copy of the T allele shifted the measure 0.053 lower (95% confidence interval 0.037-0.069); p = 6 × 10−12.
Where it sits Chromosome 13, band 13q12.13 — inside RNF6.
What each result means
C/CNo copy of the version the research linked to Fasting plasma glucose. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Fasting plasma glucose. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Fasting plasma glucose. That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature communications · 2025 · PMID 40325049 · open access
Questions about rs76154673
What is rs76154673?
rs76154673 is a single position in the genome, in or near the RNF6 gene. Published research associates it with fasting plasma glucose. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs76154673 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 rs76154673 come from?
GWAS Catalog, Nature communications 2025, PMID:40325049. 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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