KRT8

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Red KRT8 in Mendeliome Version 1.1891	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Cirrhosis, cryptogenic, MIM# 215600
Red KRT8 in Mackenzie's Mission_Reproductive Carrier Screening Level 2: Screening Version 0.109	review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Red Mackenzie's Mission Phenotypes CIRRHOSIS, FAMILIAL, MIM #215600
Red KRT8 in Additional findings_Paediatric Level 2: Screening Version 0.278	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red BabySeq Category C gene Phenotypes Cirrhosis, cryptogenic
Red KRT8 in Prepair 1000+ Level 2: Screening Version 1.9	review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Red Mackenzie's Mission Phenotypes CIRRHOSIS, FAMILIAL, MIM #215600
Red KRT8 in BabyScreen+ newborn screening Level 2: Screening Version 1.113	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources BabySeq Category C gene Expert Review Red Phenotypes Cirrhosis, cryptogenic

5 panels