NM_006772.3(SYNGAP1):c.2478C>T (p.Asp826=) AND Intellectual disability, autosomal dominant 5
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 16, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002159101.6
Allele description [Variation Report for NM_006772.3(SYNGAP1):c.2478C>T (p.Asp826=)]
NM_006772.3(SYNGAP1):c.2478C>T (p.Asp826=)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024