NM_000257.4(MYH7):c.5394C>T (p.Asp1798=) AND Left ventricular noncompaction cardiomyopathy
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 14, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000279954.12
Allele description [Variation Report for NM_000257.4(MYH7):c.5394C>T (p.Asp1798=)]
NM_000257.4(MYH7):c.5394C>T (p.Asp1798=)
Condition(s)
- Name:
- Left ventricular noncompaction cardiomyopathy
- Identifiers:
- MedGen: C4021133; Human Phenotype Ontology: HP:0011664
Assertion and evidence details
Last Updated: Oct 13, 2024