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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.
Strength of the evidence
2 / 4
Its strongest genetic-study result is p = 10−46, with 1 associations in the GWAS Catalog.
How this is scored
4: ClinVar disease-causing, reviewed by an expert panel or a guideline (3–4 stars). 3: ClinVar, several labs agreeing (2 stars), or a genetic study at p ≤ 10−50. 2: ClinVar from one lab (1 star), or p ≤ 10−20. 1: ClinVar submitted without criteria (0 stars), or genome-wide significance (p ≤ 5×10−8). The higher of the two counts. It says how solid the evidence is, not whether it matters for a particular person.
What the study found
Who was studied 90,479 African American or Afro-Caribbean individuals, 42,403 Hispanic or Latin American individuals, 3,997 East Asian ancestry individuals, 310,849 European ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.0814 higher (95% confidence interval 0.07-0.093); p = 2 × 10−46.
How common The T allele had a frequency of about 94% in the people studied.
Where it sits Chromosome 21, band 21q22.12 — in an intron of RUNX1.
What each result means
C/CNo copy of the version the research linked to eosinophil (absolute count, minimum, inv-norm transformed). This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to eosinophil (absolute count, minimum, inv-norm transformed). That is a smaller link than two copies.
T/TTwo copies of the version the research linked to eosinophil (absolute count, minimum, inv-norm transformed). That is the strongest link of the three results. A link in a study is not a diagnosis.
Science (New York, N.Y.) · 2024 · PMID 39024449 · open access
Questions about rs56285302
What is rs56285302?
rs56285302 is a single position in the genome, in or near the RUNX1 gene. Published research associates it with eosinophil (absolute count, minimum, inv-norm transformed). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs56285302 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 rs56285302 come from?
GWAS Catalog, Science (New York, N.Y.) 2024, PMID:39024449. 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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