NM_000466.3(PEX1):c.2868T>A (p.Val956=) AND Zellweger spectrum disorders
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Jan 23, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001504524.8
Allele description [Variation Report for NM_000466.3(PEX1):c.2868T>A (p.Val956=)]
NM_000466.3(PEX1):c.2868T>A (p.Val956=)
Condition(s)
Assertion and evidence details
Last Updated: Jun 23, 2024