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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 327,790 British ancestry individuals.
The effect
Each copy of the G allele shifted the measure 0.013 lower (95% confidence interval 0.0091-0.0169); p = 3 × 10−8.
How common The G allele had a frequency of about 44% in the people studied.
Where it sits Chromosome 17, band 17q24.2 — between genes, 7.2 kb from NOL11.
What each result means
C/CNo copy of the version the research linked to Leukocyte telomere length. This is the starting point the study compared everyone against.
C/GOne copy of the version the research linked to Leukocyte telomere length. That is a smaller link than two copies.
G/GTwo 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.
rs4496196 is a single position in the genome, in or near the near NOL11 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 rs4496196 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 rs4496196 come from?
GWAS Catalog, GeroScience 2024, PMID:38837026. 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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