NM_001643.2(APOA2):c.53-43TG[18] AND APOA2-related disorder
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jun 11, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003973138.1
Allele description [Variation Report for NM_001643.2(APOA2):c.53-43TG[18]]
NM_001643.2(APOA2):c.53-43TG[18]
Condition(s)
- Name:
- APOA2-related disorder
- Synonyms:
- APOA2-related condition
- Identifiers:
Assertion and evidence details
Last Updated: May 19, 2024