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Mean corpuscular volume

OR51 · rs113342804

What the study found

Who was studied 12,502 Hispanic/Latino individuals; replicated in 4,772 Hispanic/Latino individuals.

The effect Each copy of the A allele shifted the measure 2.28 fL higher (95% confidence interval 1.59-2.97); p = 9 × 10−11.

How common The A allele had a frequency of about 99% in the people studied.

Where it sits Chromosome 11, band 11p15.4 — in an intron of MMP26.

What each result means

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

Questions about rs113342804

What is rs113342804?

rs113342804 is a single position in the genome, in or near the OR51 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.

Does having rs113342804 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 rs113342804 come from?

GWAS Catalog, PLoS genetics 2017, PMID:28453575. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.

Mean corpuscular volume (rs113342804). MyGeneLog™. https://www.mygenelog.com/variants/rs113342804

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