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eosinophil (fraction, maximum, inv-norm transformed)

LARP4B · rs12360270

What the study found

Who was studied 335,542 European ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.0445 lower (95% confidence interval 0.038-0.051); p = 5 × 10−39.

How common The G allele had a frequency of about 77% in the people studied.

Where it sits Chromosome 10, band 10p15.3 — in an intron of LARP4B.

What each result means

A/A 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.
A/G One copy of the version the research linked to eosinophil (fraction, maximum, inv-norm transformed). That is a smaller link than two copies.
G/G 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 rs12360270

What is rs12360270?

rs12360270 is a single position in the genome, in or near the LARP4B 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 rs12360270 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 rs12360270 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) (rs12360270). MyGeneLog™. https://www.mygenelog.com/variants/rs12360270

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