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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 438,351 Non-Finnish European ancestry individuals.
The effect
Each copy of the G allele shifted the measure 0.0375 lower (95% confidence interval 0.026-0.049); p = 4 × 10−11.
Where it sits Chromosome 20, band 20q11.23 — in an intron of DSN1.
What each result means
A/ANo copy of the version the research linked to Telomere length (principal component 1). This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Telomere length (principal component 1). That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Telomere length (principal component 1). That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature genetics · 2024 · PMID 39192095 · open access
Questions about rs56317999
What is rs56317999?
rs56317999 is a single position in the genome, in or near the DSN1 gene. Published research associates it with telomere length (principal component 1). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs56317999 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 rs56317999 come from?
GWAS Catalog, Nature genetics 2024, PMID:39192095. 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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