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eosinophil (fraction, maximum, inv-norm transformed)

RDM1P2 · rs2667932

What the study found

Who was studied 335,542 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.0423 higher (95% confidence interval 0.035-0.049); p = 2 × 10−33.

How common The T allele had a frequency of about 74% in the people studied.

Where it sits Chromosome 17, band 17q21.31 — in an intron of RDM1P2.

What each result means

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

Questions about rs2667932

What is rs2667932?

rs2667932 is a single position in the genome, in or near the RDM1P2 gene. Published research associates it with eosinophil (fraction, maximum, 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 rs2667932 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 rs2667932 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 (fraction, maximum, inv-norm transformed) (rs2667932). MyGeneLog™. https://www.mygenelog.com/variants/rs2667932

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