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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 59,219 British, Irish ancestry individuals.
The effect
Each copy of the G allele carried 0.88 times the odds of Clonal hematopoiesis (mutational barcode method) (95% confidence interval 0.84-0.91); p = 4 × 10−12.
Where it sits Chromosome 14, band 14q32.2 — between genes, 21.6 kb from DLK1.
What each result means
A/ANo copy of the version the research linked to Clonal hematopoiesis (mutational barcode method). This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Clonal hematopoiesis (mutational barcode method). That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Clonal hematopoiesis (mutational barcode method). That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature genetics · 2023 · PMID 37932435 · open access
Questions about rs17099617
What is rs17099617?
rs17099617 is a single position in the genome, in or near the near DLK1 gene. Published research associates it with clonal hematopoiesis (mutational barcode method). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs17099617 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 rs17099617 come from?
GWAS Catalog, Nature genetics 2023, PMID:37932435. 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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