NM_174936.4(PCSK9):c.1847C>A (p.Pro616Gln) AND Familial hypercholesterolemia
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 18, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000775297.13
Allele description [Variation Report for NM_174936.4(PCSK9):c.1847C>A (p.Pro616Gln)]
NM_174936.4(PCSK9):c.1847C>A (p.Pro616Gln)
Condition(s)
Assertion and evidence details
Last Updated: Nov 10, 2024