NM_002617.4(PEX10):c.912+14C>A AND Peroxisome biogenesis disorder, complementation group 7
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 7, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002193811.5
Allele description [Variation Report for NM_002617.4(PEX10):c.912+14C>A]
NM_002617.4(PEX10):c.912+14C>A
Condition(s)
- Name:
- Peroxisome biogenesis disorder, complementation group 7 (CG7)
- Synonyms:
- Peroxisome biogenesis disorder, complementation group B
- Identifiers:
- MedGen: C1864399
-
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Last Updated: Feb 28, 2024