NM_007327.4(GRIN1):c.969-5_969-4delinsTT AND Intellectual disability, autosomal dominant 8
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 4, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002894001.2
Allele description [Variation Report for NM_007327.4(GRIN1):c.969-5_969-4delinsTT]
NM_007327.4(GRIN1):c.969-5_969-4delinsTT
Condition(s)
Assertion and evidence details
Last Updated: Feb 20, 2024