NM_000466.3(PEX1):c.2718+9T>A AND Zellweger spectrum disorders
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 9, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001395519.6
Allele description [Variation Report for NM_000466.3(PEX1):c.2718+9T>A]
NM_000466.3(PEX1):c.2718+9T>A
Condition(s)
Assertion and evidence details
Last Updated: Feb 20, 2024