NM_174936.4(PCSK9):c.267G>A (p.Ser89=) AND Cardiovascular phenotype
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 21, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003303241.2
Allele description [Variation Report for NM_174936.4(PCSK9):c.267G>A (p.Ser89=)]
NM_174936.4(PCSK9):c.267G>A (p.Ser89=)
Condition(s)
- Name:
- Cardiovascular phenotype
- Identifiers:
- MedGen: CN230736
Assertion and evidence details
Last Updated: May 7, 2024