NM_002397.5(MEF2C):c.402+9T>G AND Intellectual disability, autosomal dominant 20
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 27, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002173195.5
Allele description [Variation Report for NM_002397.5(MEF2C):c.402+9T>G]
NM_002397.5(MEF2C):c.402+9T>G
Condition(s)
Assertion and evidence details
Last Updated: Mar 5, 2024