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

NDFIP1 · rs3765011

What the study found

Who was studied 310,849 European ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.0378 lower (95% confidence interval 0.032-0.043); p = 2 × 10−39.

How common The G allele had a frequency of about 39% in the people studied.

Where it sits Chromosome 5, band 5q31.3 — in an intron of NDFIP1.

What each result means

C/C No 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/G One copy of the version the research linked to eosinophil (absolute count, minimum, inv-norm transformed). That is a smaller link than two copies.
G/G Two 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.
Source

Questions about rs3765011

What is rs3765011?

rs3765011 is a single position in the genome, in or near the NDFIP1 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 rs3765011 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 rs3765011 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, minimum, inv-norm transformed) (rs3765011). MyGeneLog™. https://www.mygenelog.com/variants/rs3765011

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