APOC3:Ensemblv90

apolipoprotein C3
OMIM: 107720, ClinGen, DECIPHER

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Red APOC3 in Mendeliome


Version 1.3802

1 review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Apolipoprotein C-III deficiency MIM#614028

Red APOC3 in Dyslipidaemia


Level 2: Endocrine disorders
Version 0.46

Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • 1 review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Red
    • Royal Melbourne Hospital
    Phenotypes
    • Apolipoprotein C-III deficiency MIM#614028

    Red APOC3 in Dyslipidaemia


    Level 2: Endocrine disorders
    Version 1.0

    1 review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Royal Melbourne Hospital
    • Expert Review Red
    Phenotypes
    • Apolipoprotein C-III deficiency MIM#614028