CACNB2

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Red CACNB2 in Brugada syndrome Level 2: Cardiovascular disorders Version 0.34 Component of the following Super Panels: Adult Cardiac SuperPanel Arrhythmia_SuperPanel	review	Unknown	Sources Expert Review Red Victorian Clinical Genetics Services Tags disputed
Red CACNB2 in Incidentalome Version 0.301	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Brugada syndrome 4, MIM# 611876 Tags cardiac
Red CACNB2 in Short QT syndrome Level 2: Cardiovascular disorders Version 1.7 Component of the following Super Panels: Adult Cardiac SuperPanel Arrhythmia_SuperPanel	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Expert Review Phenotypes Short QT syndrome 1 Tags disputed
Red CACNB2 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 Brugada syndrome
Red CACNB2 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 Brugada syndrome

5 panels