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Mean corpuscular volume

NPRL3 · rs2238368

Where this position leads

Condition: Blood Cell Counts

rs2238368 Condition: Blood Cell Counts Blood Cell Counts Condition rs2238368 rs2238368 NPRL3

What the study found

Who was studied 172,433 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.0754 lower (95% confidence interval 0.068-0.082); p = 6 × 10−101.

How common The T allele had a frequency of about 46% in the people studied.

Where it sits Chromosome 16, band 16p13.3 — in an intron of NPRL3.

What each result means

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

Questions about rs2238368

What is rs2238368?

rs2238368 is a single position in the genome, in or near the NPRL3 gene. Published research associates it with mean corpuscular volume. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs2238368 linked to?

On MyGeneLog this position is linked to Blood Cell Counts. The research behind each link, and its sources, are set out on that condition page.

Does having rs2238368 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 rs2238368 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 corpuscular volume (rs2238368). MyGeneLog™. https://www.mygenelog.com/variants/rs2238368

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