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Hypertrophic cardiomyopathy (ICD-10 coded)

PARD3B · rs188937806

Where this position leads

Condition: Hypertrophic Cardiomyopathy

rs188937806 Condition: Hypertrophic Cardiomyopathy Hypertrophic Cardiomyopathy Condition rs188937806 rs188937806 PARD3B

What the study found

Who was studied 305 European ancestry cases, 11 African ancestry cases, 7 Caribbean ancestry cases, 40 cases, 7,260 European, African, Asian or unknown ancestry controls.

The effect The reported allele is T; the catalogue records no effect size ; p = 1 × 10−8.

Where it sits Chromosome 2, band 2q33.3 — in an intron of PARD3B.

What each result means

C/C No copy of the version the research linked to Hypertrophic cardiomyopathy (ICD-10 coded). This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Hypertrophic cardiomyopathy (ICD-10 coded). That is a smaller link than two copies.
T/T Two copies of the version the research linked to Hypertrophic cardiomyopathy (ICD-10 coded). That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs188937806

What is rs188937806?

rs188937806 is a single position in the genome, in or near the PARD3B gene. Published research associates it with hypertrophic cardiomyopathy (icd-10 coded). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs188937806 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 rs188937806 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 rs188937806 come from?

GWAS Catalog, Frontiers in genetics 2022, PMID:35685441. 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.

Hypertrophic cardiomyopathy (ICD-10 coded) (rs188937806). MyGeneLog™. https://www.mygenelog.com/variants/rs188937806

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