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Who was studied 3,100 European ancestry cases, 7,667 European ancestry controls; replicated in 1,958 cases, 5,530 controls.
The effect
Each copy of the A allele carried 1.32 times the odds of Chronic lymphocytic leukemia (95% confidence interval 1.23-1.41); p = 6 × 10−16.
How common The A allele had a frequency of about 54% in the people studied.
Where it sits Chromosome 6, band 6p21.32 — between genes, 10.7 kb from HLA-DRB1.
What each result means
A/ATwo copies of the version the research linked to Chronic lymphocytic leukemia. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/GOne copy of the version the research linked to Chronic lymphocytic leukemia. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Chronic lymphocytic leukemia. This is the starting point the study compared everyone against.
Nature communications · 2016 · PMID 26956414 · open access
Questions about rs9270750
What is rs9270750?
rs9270750 is a single position in the genome, in or near the HLA-DQB1 gene. Published research associates it with chronic lymphocytic leukemia. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs9270750 linked to?
On MyGeneLog this position is linked to Chronic Lymphocytic Leukaemia. The research behind each link, and its sources, are set out on that condition page.
Does having rs9270750 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 rs9270750 come from?
GWAS Catalog, Nature communications 2016, PMID:26956414. 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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