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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 9,598 Hispanic or Latin American individuals.
The effect
Each copy of the C allele shifted the measure 0.153 higher (95% confidence interval 0.12-0.187); p = 2 × 10−19.
How common The C allele had a frequency of about 7% in the people studied.
Where it sits Chromosome 10, band 10q24.33 — between genes, 2.1 kb from STN1.
What each result means
C/CTwo copies of the version the research linked to Leukocyte telomere length. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/TOne copy of the version the research linked to Leukocyte telomere length. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Leukocyte telomere length. This is the starting point the study compared everyone against.
Nature genetics · 2025 · PMID 39948438 · open access
Questions about rs12415148
What is rs12415148?
rs12415148 is a single position in the genome, in or near the near STN1 gene. Published research associates it with leukocyte telomere length. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs12415148 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 rs12415148 come from?
GWAS Catalog, Nature genetics 2025, PMID:39948438. 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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