NM_174936.4(PCSK9):c.516G>A (p.Gln172=) AND Hypercholesterolemia, autosomal dominant, 3
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 15, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003096640.2
Allele description [Variation Report for NM_174936.4(PCSK9):c.516G>A (p.Gln172=)]
NM_174936.4(PCSK9):c.516G>A (p.Gln172=)
Condition(s)
Assertion and evidence details
Last Updated: May 1, 2024