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Mean platelet volume

ZNF324B · rs11671005

What the study found

Who was studied 164,454 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.0272 lower (95% confidence interval 0.019-0.035); p = 1 × 10−10.

How common The A allele had a frequency of about 26% in the people studied.

Where it sits Chromosome 19, band 19q13.43 — in an intron of ZNF324B.

What each result means

A/A Two copies of the version the research linked to Mean platelet volume. 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 Mean platelet volume. That is a smaller link than two copies.
G/G No copy of the version the research linked to Mean platelet volume. This is the starting point the study compared everyone against.
Source

Questions about rs11671005

What is rs11671005?

rs11671005 is a single position in the genome, in or near the ZNF324B gene. Published research associates it with mean platelet volume. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs11671005 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 rs11671005 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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Mean platelet volume (rs11671005). MyGeneLog™. https://www.mygenelog.com/variants/rs11671005

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