NM_174936.4(PCSK9):c.123G>C (p.Leu41=) AND Familial hypercholesterolemia
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 25, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001186114.2
Allele description [Variation Report for NM_174936.4(PCSK9):c.123G>C (p.Leu41=)]
NM_174936.4(PCSK9):c.123G>C (p.Leu41=)
Condition(s)
Assertion and evidence details
Last Updated: Sep 1, 2024