NM_006772.3(SYNGAP1):c.3583-17G>A AND Intellectual disability, autosomal dominant 5
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 25, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002073071.6
Allele description [Variation Report for NM_006772.3(SYNGAP1):c.3583-17G>A]
NM_006772.3(SYNGAP1):c.3583-17G>A
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024