NM_174936.4(PCSK9):c.267G>A (p.Ser89=) AND Hypercholesterolemia, autosomal dominant, 3
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Dec 18, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000864864.9
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)
Assertion and evidence details
Last Updated: May 7, 2024