APOC2

apolipoprotein C2
OMIM: 608083, ClinGen, DECIPHER

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Green APOC2 in Mendeliome


Version 2.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Hyperlipoproteinemia, type Ib MIM#207750

Amber APOC2 in Amyloidosis


Version 2.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • APOC2-related amyloidosis, MONDO:0019065

Green APOC2 in Dyslipidaemia


Level 2: Endocrine disorders; Cardiovascular disorders
Version 1.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Royal Melbourne Hospital
Phenotypes
  • Hyperlipoproteinemia, type Ib MIM#207750

Green APOC2 in Transplant Co-Morbidity


Level 2: Screening
Version 1.0

0 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Royal Melbourne Hospital
Phenotypes
  • Hyperlipoproteinemia, type Ib MIM#207750