NM_007327.4(GRIN1):c.793+20G>C AND Intellectual disability, autosomal dominant 8
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 10, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003643922.2
Allele description [Variation Report for NM_007327.4(GRIN1):c.793+20G>C]
NM_007327.4(GRIN1):c.793+20G>C
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024