NM_001110792.2(MECP2):c.6CGC[5] (p.Ala8del) AND Inborn genetic diseases
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 9, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002313582.8
Allele description [Variation Report for NM_001110792.2(MECP2):c.6CGC[5] (p.Ala8del)]
NM_001110792.2(MECP2):c.6CGC[5] (p.Ala8del)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Apr 20, 2024