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Neutrophil count

DNAJC13 · rs112880875

What the study found

Who was studied 519,288 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.0268 SD unit higher (95% confidence interval 0.02-0.033); p = 1 × 10−15.

How common The A allele had a frequency of about 9% in the people studied.

Where it sits Chromosome 3, band 3q22.1 — in an intron of DNAJC13.

What each result means

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

Questions about rs112880875

What is rs112880875?

rs112880875 is a single position in the genome, in or near the DNAJC13 gene. Published research associates it with neutrophil count. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs112880875 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 rs112880875 come from?

GWAS Catalog, Cell 2020, PMID:32888493. 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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Neutrophil count (rs112880875). MyGeneLog™. https://www.mygenelog.com/variants/rs112880875

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