APOA2

apolipoprotein A2
OMIM: 107670, ClinGen, DECIPHER

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Red APOA2 in Mendeliome


Version 1.4559

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