NM_000384.3(APOB):c.7612C>T (p.Leu2538=) AND Hypercholesterolemia, autosomal dominant, type B
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001094633.12
Allele description [Variation Report for NM_000384.3(APOB):c.7612C>T (p.Leu2538=)]
NM_000384.3(APOB):c.7612C>T (p.Leu2538=)
Condition(s)
- Name:
- Hypercholesterolemia, autosomal dominant, type B (FHCL2)
- Synonyms:
- APOLIPOPROTEIN B-100, FAMILIAL DEFECTIVE; APOLIPOPROTEIN B-100, FAMILIAL LIGAND-DEFECTIVE; HYPERCHOLESTEROLEMIA, FAMILIAL, DUE TO LIGAND-DEFECTIVE APOLIPOPROTEIN B; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0007751; MedGen: C1704417; OMIM: 144010
Assertion and evidence details
Last Updated: Sep 29, 2024