NM_001351132.2(PEX5):c.1718+18G>C AND Peroxisome biogenesis disorder 2B
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 25, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003602574.2
Allele description [Variation Report for NM_001351132.2(PEX5):c.1718+18G>C]
NM_001351132.2(PEX5):c.1718+18G>C
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024