NM_000384.3(APOB):c.13651T>C (p.Tyr4551His) AND Cardiovascular phenotype
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 22, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002386356.9
Allele description [Variation Report for NM_000384.3(APOB):c.13651T>C (p.Tyr4551His)]
NM_000384.3(APOB):c.13651T>C (p.Tyr4551His)
Condition(s)
- Name:
- Cardiovascular phenotype
- Identifiers:
- MedGen: CN230736
Assertion and evidence details
Last Updated: Nov 24, 2024