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Hypertrophic cardiomyopathy

PRG3 · rs764568652

Where this position leads

Condition: Hypertrophic Cardiomyopathy

rs764568652 Condition: Hypertrophic Cardiomyopathy Hypertrophic Cardiomyopathy Condition rs764568652 rs764568652 PRG3

What the study found

Who was studied 507 European ancestry cases, 489,220 European ancestry controls, 383 East Asian ancestry cases, 177,745 East Asian ancestry controls.

The effect Each copy of the G allele shifted the measure 65.3 higher (95% confidence interval 52.92-77.6); p = 3 × 10−25.

Where it sits Chromosome 11, band 11q12.1 — in an intron of PRG3.

What each result means

A/A No copy of the version the research linked to Hypertrophic cardiomyopathy. This is the starting point the study compared everyone against.
A/G One copy of the version the research linked to Hypertrophic cardiomyopathy. That is a smaller link than two copies.
G/G Two copies of the version the research linked to Hypertrophic cardiomyopathy. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs764568652

What is rs764568652?

rs764568652 is a single position in the genome, in or near the PRG3 gene. Published research associates it with hypertrophic cardiomyopathy. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs764568652 linked to?

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

Does having rs764568652 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 rs764568652 come from?

GWAS Catalog, Nature genetics 2021, PMID:34594039. 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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Hypertrophic cardiomyopathy (rs764568652). MyGeneLog™. https://www.mygenelog.com/variants/rs764568652

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