NM_000483.5(APOC2):c.-2C>T AND APOC2-related disorder
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Dec 7, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003940316.2
Allele description [Variation Report for NM_000483.5(APOC2):c.-2C>T]
NM_000483.5(APOC2):c.-2C>T
Condition(s)
- Name:
- APOC2-related disorder
- Synonyms:
- APOC2-related condition
- Identifiers:
Assertion and evidence details
Last Updated: Oct 8, 2024