NM_174936.4(PCSK9):c.45GCT[9] (p.Leu22_Leu23dup) AND Familial hypercholesterolemia
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 29, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000776036.10
Allele description [Variation Report for NM_174936.4(PCSK9):c.45GCT[9] (p.Leu22_Leu23dup)]
NM_174936.4(PCSK9):c.45GCT[9] (p.Leu22_Leu23dup)
Condition(s)
Assertion and evidence details
Last Updated: Jun 2, 2024