NM_000466.3(PEX1):c.1360-4G>T AND Zellweger spectrum disorders
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 1, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001450061.7
Allele description [Variation Report for NM_000466.3(PEX1):c.1360-4G>T]
NM_000466.3(PEX1):c.1360-4G>T
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024