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eosinophil (absolute count, mean, inv-norm transformed)

IRAK2 · rs563913827

What the study found

Who was studied 90,448 African American or Afro-Caribbean individuals.

The effect Each copy of the A allele shifted the measure 0.111 lower (95% confidence interval 0.086-0.135); p = 8 × 10−19.

How common The A allele had a frequency of about 95% in the people studied.

Where it sits Chromosome 3, band 3p25.3 — in an intron of IRAK2.

What each result means

A/A Two copies of the version the research linked to eosinophil (absolute count, mean, inv-norm transformed). That is the strongest link of the three results. A link in a study is not a diagnosis.
A/T One copy of the version the research linked to eosinophil (absolute count, mean, inv-norm transformed). That is a smaller link than two copies.
T/T No copy of the version the research linked to eosinophil (absolute count, mean, inv-norm transformed). This is the starting point the study compared everyone against.
Source

Questions about rs563913827

What is rs563913827?

rs563913827 is a single position in the genome, in or near the IRAK2 gene. Published research associates it with eosinophil (absolute count, mean, 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 rs563913827 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 rs563913827 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.

Quoting this page

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eosinophil (absolute count, mean, inv-norm transformed) (rs563913827). MyGeneLog™. https://www.mygenelog.com/variants/rs563913827

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