NM_006772.3(SYNGAP1):c.865A>G (p.Met289Val) AND Intellectual disability, autosomal dominant 5
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Sep 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003047028.2
Allele description [Variation Report for NM_006772.3(SYNGAP1):c.865A>G (p.Met289Val)]
NM_006772.3(SYNGAP1):c.865A>G (p.Met289Val)
Condition(s)
Assertion and evidence details
Last Updated: Feb 20, 2024