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Red cell distribution width

BC030525 · rs10479001

Where this position leads

Condition: Blood Cell Counts

rs10479001 Condition: Blood Cell Counts Blood Cell Counts Condition rs10479001 rs10479001 BC030525

What the study found

Who was studied 116,666 British ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.0564 higher (95% confidence interval 0.037-0.076); p = 1 × 10−8.

How common The T allele had a frequency of about 4% in the people studied.

Where it sits Chromosome 5, band 5q31.1 — a missense change in P4HA2.

What each result means

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

Questions about rs10479001

What is rs10479001?

rs10479001 is a single position in the genome, in or near the BC030525 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 rs10479001 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 rs10479001 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 rs10479001 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 (rs10479001). MyGeneLog™. https://www.mygenelog.com/variants/rs10479001

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