NM_002024.6(FMR1):c.1572C>T (p.Ser524=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 8, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002317683.8
Allele description [Variation Report for NM_002024.6(FMR1):c.1572C>T (p.Ser524=)]
NM_002024.6(FMR1):c.1572C>T (p.Ser524=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Apr 20, 2024