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Cardiomyopathy (PheCode 425)

DDB2 · rs73467637

Where this position leads

Condition: Cardiomyopathy

rs73467637 Condition: Cardiomyopathy Cardiomyopathy Condition rs73467637 rs73467637 DDB2

What the study found

Who was studied 7,053 African American or Afro-Caribbean cases, 111,507 African American or Afro-Caribbean controls, 20,680 European ancestry cases, 418,334 European ancestry controls, 1,730 Hispanic or Latin American cases, 57,089 Hispanic or Latin American controls.

The effect Each copy of the A allele shifted the measure 0.31 lower (95% confidence interval 0.26-0.36); p = 4 × 10−16.

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

Where it sits Chromosome 11, band 11p11.2 — in an intron of DDB2.

What each result means

A/A Two copies of the version the research linked to Cardiomyopathy (PheCode 425). 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 Cardiomyopathy (PheCode 425). That is a smaller link than two copies.
G/G No copy of the version the research linked to Cardiomyopathy (PheCode 425). This is the starting point the study compared everyone against.
Source

Questions about rs73467637

What is rs73467637?

rs73467637 is a single position in the genome, in or near the DDB2 gene. Published research associates it with cardiomyopathy (phecode 425). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs73467637 linked to?

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

Does having rs73467637 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 rs73467637 come from?

GWAS Catalog, Science (New York, N.Y.) 2024, PMID:39024449. 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.

Cardiomyopathy (PheCode 425) (rs73467637). MyGeneLog™. https://www.mygenelog.com/variants/rs73467637

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