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Red cell distribution width

TNPO1 · rs266428

Where this position leads

Condition: Blood Cell Counts

rs266428 Condition: Blood Cell Counts Blood Cell Counts Condition rs266428 rs266428 TNPO1

What the study found

Who was studied 116,666 British ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.0269 lower (95% confidence interval 0.018-0.035); p = 4 × 10−12.

Where it sits Chromosome 5, band 5q13.2 — in an intron of TNPO1.

What each result means

A/A Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Red cell distribution width compared to the general population.
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Red cell distribution width.
G/G Published research associates this genotype with typical/baseline likelihood of Red cell distribution width — no copies of the reported risk allele.
Source

Questions about rs266428

What is rs266428?

rs266428 is a single position in the genome, in or near the TNPO1 gene. Published research associates it with red cell distribution width. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs266428 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 rs266428 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 rs266428 come from?

GWAS Catalog, PLoS One 2017, PMID:28957414. 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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Red cell distribution width (rs266428). MyGeneLog™. https://www.mygenelog.com/variants/rs266428

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