NM_001165963.4(SCN1A):c.5418G>A (p.Glu1806=) AND Inborn genetic diseases
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Mar 13, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002311584.9
Allele description [Variation Report for NM_001165963.4(SCN1A):c.5418G>A (p.Glu1806=)]
NM_001165963.4(SCN1A):c.5418G>A (p.Glu1806=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Jun 9, 2024