NM_007327.4(GRIN1):c.2241G>C (p.Val747=) AND Inborn genetic diseases
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Mar 2, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002312119.9
Allele description [Variation Report for NM_007327.4(GRIN1):c.2241G>C (p.Val747=)]
NM_007327.4(GRIN1):c.2241G>C (p.Val747=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Oct 13, 2024