NM_002156.5(HSPD1):c.700+8C>T AND Spastic paraplegia
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Oct 24, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001088313.7
Allele description [Variation Report for NM_002156.5(HSPD1):c.700+8C>T]
NM_002156.5(HSPD1):c.700+8C>T
Condition(s)
- Name:
- Spastic paraplegia
- Identifiers:
- MedGen: C0037772; Human Phenotype Ontology: HP:0001258
Assertion and evidence details
Last Updated: Mar 16, 2024