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Hypertrophic cardiomyopathy

ARHGAP1 · rs187474069

Where this position leads

Condition: Hypertrophic Cardiomyopathy

rs187474069 Condition: Hypertrophic Cardiomyopathy Hypertrophic Cardiomyopathy Condition rs187474069 rs187474069 ARHGAP1

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 C allele shifted the measure 56.1 higher (95% confidence interval 45.28-66.83); p = 2 × 10−24.

Where it sits Chromosome 11, band 11p11.2 — in an intron of ARHGAP1.

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/C One copy of the version the research linked to Hypertrophic cardiomyopathy. That is a smaller link than two copies.
C/C 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 rs187474069

What is rs187474069?

rs187474069 is a single position in the genome, in or near the ARHGAP1 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 rs187474069 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 rs187474069 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 rs187474069 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 (rs187474069). MyGeneLog™. https://www.mygenelog.com/variants/rs187474069

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