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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 840 African American child cases, 3,360 African American child controls.
The effect
Each copy of the A allele carried 1.62 times the odds of B-cell acute lymphoblastic leukaemia (95% confidence interval 1.49-1.74); p = 3 × 10−14.
Where it sits Chromosome 7, band 7p12.2 — between genes, 4.9 kb from IKZF1.
What each result means
A/ATwo copies of the version the research linked to B-cell acute lymphoblastic leukaemia. 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 B-cell acute lymphoblastic leukaemia. That is a smaller link than two copies.
G/GNo copy of the version the research linked to B-cell acute lymphoblastic leukaemia. This is the starting point the study compared everyone against.
Nature communications · 2025 · PMID 41125582 · open access
Questions about rs17133807
What is rs17133807?
rs17133807 is a single position in the genome, in or near the near IKZF1 gene. Published research associates it with b-cell acute lymphoblastic leukaemia. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs17133807 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 rs17133807 come from?
GWAS Catalog, Nature communications 2025, PMID:41125582. 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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