NM_000384.3(APOB):c.6636TGA[1] (p.Asp2213del) AND not provided
- Germline classification:
- Benign/Likely benign (4 submissions)
- Last evaluated:
- Jul 1, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000471850.40
Allele description [Variation Report for NM_000384.3(APOB):c.6636TGA[1] (p.Asp2213del)]
NM_000384.3(APOB):c.6636TGA[1] (p.Asp2213del)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Aug 18, 2024