NC_012920.1:m.7496T>C AND Myopathy
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 21, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000408943.1
Allele description [Variation Report for NC_012920.1:m.7496T>C]
NC_012920.1:m.7496T>C
Condition(s)
- Name:
- Myopathy
- Synonyms:
- Muscle disorders
- Identifiers:
- MONDO: MONDO:0005336; MeSH: D009135; MedGen: C0026848; Human Phenotype Ontology: HP:0003198
Assertion and evidence details
Last Updated: Feb 7, 2023