NM_004068.4(AP2M1):c.74+485G>T AND AP2M1-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 2, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003901013.1
Allele description [Variation Report for NM_004068.4(AP2M1):c.74+485G>T]
NM_004068.4(AP2M1):c.74+485G>T
Condition(s)
- Name:
- AP2M1-related disorder
- Synonyms:
- AP2M1-related condition
- Identifiers:
Assertion and evidence details
Last Updated: Jun 17, 2024