NM_001131005.2(MEF2C):c.*2771T>G AND Intellectual Disability, Stereotypic Movements, Epilepsy, and/or Cerebral Malformations
- 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:
- RCV000290992.1
Allele description
NM_001131005.2(MEF2C):c.*2771T>G
Condition(s)
- Name:
- Intellectual Disability, Stereotypic Movements, Epilepsy, and/or Cerebral Malformations
- Identifiers:
- MedGen: CN239216
Assertion and evidence details
Last Updated: Nov 2, 2019