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Mitochondrial DNA copy number

GNB4 · rs13088724

What the study found

Who was studied 395,718 British, Irish, Other White, South Asian, African ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.0175 higher (95% confidence interval 0.012-0.023); p = 8 × 10−12.

How common The A allele had a frequency of about 14% in the people studied.

Where it sits Chromosome 3, band 3q26.33 — in an intron of GNB4.

What each result means

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

Questions about rs13088724

What is rs13088724?

rs13088724 is a single position in the genome, in or near the GNB4 gene. Published research associates it with mitochondrial dna copy number. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs13088724 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 rs13088724 come from?

GWAS Catalog, eLife 2022, PMID:35023831. 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.

Mitochondrial DNA copy number (rs13088724). MyGeneLog™. https://www.mygenelog.com/variants/rs13088724

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