NM_001351132.2(PEX5):c.1110+18C>T AND Peroxisome biogenesis disorder 2B
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 16, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002081941.7
Allele description [Variation Report for NM_001351132.2(PEX5):c.1110+18C>T]
NM_001351132.2(PEX5):c.1110+18C>T
Condition(s)
Assertion and evidence details
Last Updated: Feb 16, 2025