GLYR1

glyoxylate reductase 1 homolog
OMIM: 610660, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Amber GLYR1 in Congenital Heart Defect


Level 2: Cardiovascular disorders
Version 1.33

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Literature
  • Expert Review Amber
  • Expert Review Amber
  • Literature
Phenotypes
  • Congenital heart disease (MONDO:0005453), GLYR1-related

Amber GLYR1 in Mendeliome


Version 2.516

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Congenital heart disease (MONDO:0005453), GLYR1-related