NM_000533.5(PLP1):c.5-15C>G AND Hereditary spastic paraplegia 2
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 7, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003839219.1
Allele description [Variation Report for NM_000533.5(PLP1):c.5-15C>G]
NM_000533.5(PLP1):c.5-15C>G
Condition(s)
Assertion and evidence details
Last Updated: Mar 5, 2024