NM_001378120.1(MBD5):c.4963-2A>T AND Intellectual disability, autosomal dominant 1
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 4, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001809222.1
Allele description [Variation Report for NM_001378120.1(MBD5):c.4963-2A>T]
NM_001378120.1(MBD5):c.4963-2A>T
Condition(s)
Assertion and evidence details
Last Updated: Dec 24, 2023