NM_174936.4(PCSK9):c.114C>T (p.Tyr38=) AND Hypercholesterolemia, autosomal dominant, 3
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 18, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002654995.2
Allele description [Variation Report for NM_174936.4(PCSK9):c.114C>T (p.Tyr38=)]
NM_174936.4(PCSK9):c.114C>T (p.Tyr38=)
Condition(s)
Assertion and evidence details
Last Updated: Feb 20, 2024