APOA2:Ensemblv90

apolipoprotein A2
OMIM: 107670, ClinGen, DECIPHER

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Red APOA2 in Vasculitis


Level 2: Immunological disorders
Version 0.95

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Apolipoprotein A-II deficiency
  • {Hypercholesterolemia, familial, modifier of} MIM#143890

Red APOA2 in Mendeliome


Version 1.3802

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Apolipoprotein A-II deficiency
  • {Hypercholesterolemia, familial, modifier of} MIM#143890

Red APOA2 in Vasculitis


Level 2: Immunological disorders
Version 1.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Victorian Clinical Genetics Services
  • Expert Review Red
Phenotypes
  • Apolipoprotein A-II deficiency
  • {Hypercholesterolemia, familial, modifier of} MIM#143890