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Reticulocyte fraction of red cells

CD2AP · rs9367279

What the study found

Who was studied 170,690 European ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.0268 higher (95% confidence interval 0.019-0.035); p = 2 × 10−11.

How common The G allele had a frequency of about 27% in the people studied.

Where it sits Chromosome 6, band 6p12.3 — in an intron of CD2AP.

What each result means

A/A No copy of the version the research linked to Reticulocyte fraction of red cells. This is the starting point the study compared everyone against.
A/G One copy of the version the research linked to Reticulocyte fraction of red cells. That is a smaller link than two copies.
G/G Two copies of the version the research linked to Reticulocyte fraction of red cells. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs9367279

What is rs9367279?

rs9367279 is a single position in the genome, in or near the CD2AP gene. Published research associates it with reticulocyte fraction of red cells. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs9367279 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 rs9367279 come from?

GWAS Catalog, Cell 2016, PMID:27863252. 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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Reticulocyte fraction of red cells (rs9367279). MyGeneLog™. https://www.mygenelog.com/variants/rs9367279

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