NM_000533.5(PLP1):c.191+19A>T AND Hereditary spastic paraplegia 2
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 16, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003623886.1
Allele description [Variation Report for NM_000533.5(PLP1):c.191+19A>T]
NM_000533.5(PLP1):c.191+19A>T
Condition(s)
Assertion and evidence details
Last Updated: Feb 28, 2024