Standard

Hypertrophic cardiomyopathy

MYBPC3 · rs200411226

Where this position leads

Strength of the evidence

4 / 4

ClinVar classifies it as disease-causing (or likely), reviewed at 3 of 4 stars.

How this is scored

4: ClinVar disease-causing, reviewed by an expert panel or a guideline (3–4 stars). 3: ClinVar, several labs agreeing (2 stars), or a genetic study at p ≤ 10⁻⁵⁰. 2: ClinVar from one lab (1 star), or p ≤ 10⁻²⁰. 1: ClinVar submitted without criteria (0 stars), or genome-wide significance (p ≤ 5×10⁻⁸). The higher of the two counts. It says how solid the evidence is, not whether it matters for a particular person.

What ClinVar records

Classification Likely pathogenic for Hypertrophic cardiomyopathy, Primary familial hypertrophic cardiomyopathy, Hypertrophic cardiomyopathy 4, Cardiovascular phenotype, Left ventricular noncompaction 10 and 3 more; reviewed by expert panel (3 of 4 stars, 43 submitters), last evaluated 2025-11-14. ClinVar record 164113 NM_000256.3(MYBPC3):c.1484G>A (p.Arg495Gln)

Classification Conflicting classifications of pathogenicity for Cardiomyopathy, Hypertrophic cardiomyopathy; criteria provided, conflicting classifications (1 of 4 stars, 3 submitters), last evaluated 2025-12-19. ClinVar record 915779 NM_000256.3(MYBPC3):c.1484G>T (p.Arg495Leu)

Change history MyGeneLog™ keeps a copy of every weekly release from 2026-10-19 and compares them. This position's classification has not changed since.

What this is ClinVar's aggregate record for this position (as of its 2026-10-19 release), not a result about you. A classification describes the variant against the condition named, as laboratories submitted it. Whether a person carries this variant, and what that would mean for them, is a question for a clinical test and a genetic counsellor.

What each result means

C/C No copy of the version ClinVar lists as likely disease-causing for Hypertrophic cardiomyopathy. This is the usual result. (ClinVar VCV000164113, reviewed by expert panel)

C/T One copy of the version ClinVar lists as likely disease-causing for Hypertrophic cardiomyopathy. Some conditions need only one copy; for others, one copy makes a person a carrier who is usually healthy but can pass it on. A genetic counsellor can say which applies. (ClinVar VCV000164113, reviewed by expert panel)

T/T Two copies of the version ClinVar lists as likely disease-causing for Hypertrophic cardiomyopathy. A result like this should be confirmed by a medical genetic test and talked through with a doctor; consumer DNA files can misread rare variants. (ClinVar VCV000164113, reviewed by expert panel)

Source: ClinVar VCV000164113, reviewed by expert panel

Questions about rs200411226

What is rs200411226?

rs200411226 is a single position in the genome, in or near the MYBPC3 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 rs200411226 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 rs200411226 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 rs200411226 come from?

ClinVar VCV000164113, reviewed by expert panel. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

Licensed CC BY-NC 4.0: free to read, share and adapt for non-commercial use, naming MyGeneLog™ and linking the exact page. Commercial use, including training or serving a commercial AI system, needs a licence — https://www.mygenelog.com/license

Hypertrophic cardiomyopathy (rs200411226). MyGeneLog™. https://www.mygenelog.com/variants/rs200411226

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