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Granulocyte percentage of myeloid white cells

near MIR5702 · rs35669853

What the study found

Who was studied 169,545 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.0305 lower (95% confidence interval 0.022-0.039); p = 2 × 10−11.

How common The A allele had a frequency of about 19% in the people studied.

Where it sits Chromosome 2, band 2q36.3 — between genes, 235.7 kb from MIR5702.

What each result means

A/A Two copies of the version the research linked to Granulocyte percentage of myeloid white cells. 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 Granulocyte percentage of myeloid white cells. That is a smaller link than two copies.
G/G No copy of the version the research linked to Granulocyte percentage of myeloid white cells. This is the starting point the study compared everyone against.
Source

Questions about rs35669853

What is rs35669853?

rs35669853 is a single position in the genome, in or near the near MIR5702 gene. Published research associates it with granulocyte percentage of myeloid white cells. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs35669853 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 rs35669853 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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Granulocyte percentage of myeloid white cells (rs35669853). MyGeneLog™. https://www.mygenelog.com/variants/rs35669853

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