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Standard

Cardiomyopathy, dilated, with wooly hair, keratoderma, and tooth agenesis

DSP · rs2113666898

Strength of the evidence

3 / 4

ClinVar classifies it as disease-causing (or likely), reviewed at 2 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 Pathogenic for Cardiomyopathy, dilated, with wooly hair, keratoderma, and tooth agenesis, Arrhythmogenic cardiomyopathy with wooly hair and keratoderma, Arrhythmogenic right ventricular dysplasia 8, Familial isolated arrhythmogenic right ventricular dysplasia; criteria provided, multiple submitters, no conflicts (2 of 4 stars, 3 submitters), last evaluated 2026-05-11. ClinVar record 1012338 NM_004415.4(DSP):c.748C>T (p.Gln250Ter)

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 disease-causing for Cardiomyopathy, dilated, with wooly hair, keratoderma, and tooth agenesis. This is the usual result. (ClinVar VCV001012338, criteria provided, multiple submitters, no conflicts)
C/T One copy of the version ClinVar lists as disease-causing for Cardiomyopathy, dilated, with wooly hair, keratoderma, and tooth agenesis. 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 VCV001012338, criteria provided, multiple submitters, no conflicts)
T/T Two copies of the version ClinVar lists as disease-causing for Cardiomyopathy, dilated, with wooly hair, keratoderma, and tooth agenesis. 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 VCV001012338, criteria provided, multiple submitters, no conflicts)

Source: ClinVar VCV001012338, criteria provided, multiple submitters, no conflicts

Quoting this page

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Cardiomyopathy, dilated, with wooly hair, keratoderma, and tooth agenesis (rs2113666898). MyGeneLog™. https://www.mygenelog.com/variants/rs2113666898

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