GLIS2

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Amber GLIS2 in Ciliopathies Level 2: Dysmorphic and congenital abnormality syndromes Version 1.54	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Victorian Clinical Genetics Services Phenotypes Nephronophthisis 7, OMIM#611498 MONDO:0012680
Amber GLIS2 in Mendeliome Version 1.1902	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Victorian Clinical Genetics Services Phenotypes Nephronophthisis 7, OMIM#611498 MONDO:0012680
Amber GLIS2 in Renal Ciliopathies and Nephronophthisis Level 2: Renal and urinary tract disorders Version 1.22 Component of the following Super Panels: Kidneyome_SuperPanel Renal Cystic Disease_SuperPanel	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber KidGen_CilioNephronop v38.1.0 Phenotypes Nephronophthisis 7, OMIM#611498 MONDO:0012680
Red GLIS2 in Skeletal dysplasia Level 3: Skeletal dysplasias Level 2: Skeletal disorders Version 0.285	review	Not set	Sources Expert Review Amber Emory Genetics Laboratory Victorian Clinical Genetics Services
Amber GLIS2 in Fetal anomalies Version 1.255	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Genomics England PanelApp KidGen_CilioNephronop v38.1.0 Phenotypes Nephronophthisis 7, OMIM#611498 MONDO:0012680

5 panels