NM_024306.5(FA2H):c.198G>C (p.Pro66=) AND Spastic paraplegia
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 27, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000866770.8
Allele description [Variation Report for NM_024306.5(FA2H):c.198G>C (p.Pro66=)]
NM_024306.5(FA2H):c.198G>C (p.Pro66=)
Condition(s)
- Name:
- Spastic paraplegia
- Identifiers:
- MedGen: C0037772; Human Phenotype Ontology: HP:0001258
Assertion and evidence details
Last Updated: Feb 20, 2024