NM_174936.4(PCSK9):c.996+6T>G AND Familial hypercholesterolemia
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003582148.1
Allele description [Variation Report for NM_174936.4(PCSK9):c.996+6T>G]
NM_174936.4(PCSK9):c.996+6T>G
Condition(s)
Assertion and evidence details
Last Updated: Feb 20, 2024