RYR2

ryanodine receptor 2
OMIM: 180902, ClinGen, DECIPHER

10 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 10 panels
Red RYR2 in Arrhythmogenic Cardiomyopathy Level 2: Cardiovascular disorders Version 0.68 Component of the following Super Panels: Adult Cardiac SuperPanel Arrhythmia_SuperPanel Cardiomyopathy_Adult_SuperPanel	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Arrhythmogenic right ventricular dysplasia 2, MIM# 600996 Tags refuted
Green RYR2 in Catecholaminergic Polymorphic Ventricular Tachycardia Level 2: Cardiovascular disorders Version 0.35 Component of the following Super Panels: Adult Cardiac SuperPanel Arrhythmia_SuperPanel	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Ventricular tachycardia, catecholaminergic polymorphic, 1 604772
Red RYR2 in Hypertrophic cardiomyopathy_HCM Level 2: Cardiovascular disorders Version 1.0 Component of the following Super Panels: Adult Cardiac SuperPanel Cardiomyopathy_Adult_SuperPanel	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Red Literature Phenotypes Hypertrophic cardiomyopathy
Green RYR2 in Incidentalome Version 0.318	3 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Literature Victorian Clinical Genetics Services Victorian Clinical Genetics Services Phenotypes Ventricular tachycardia, catecholaminergic polymorphic, 1, MIM# 604772 Arrhythmogenic right ventricular dysplasia 2, MIM# 600996 Hypertrophic cardiomyopathy Tags cardiac
Green RYR2 in Additional findings_Adult Level 2: Screening Version 0.169	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Melbourne Genomics Health Alliance Phenotypes Arrhythmogenic right ventricular dysplasia 2 , MIM#600996 Ventricular tachycardia, catecholaminergic polymorphic, 1, MIM# 604772
Green RYR2 in Cardiomyopathy_Paediatric Level 2: Cardiovascular disorders Version 0.196	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Literature Expert Review Green South West GLH NHS GMS Phenotypes Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, With Or Without Atrial Dysfunction And/or Dilated Cardiomyopathy Arrhythmogenic right ventricular dysplasia 2, 600996
Green RYR2 in Additional findings_Paediatric Level 2: Screening Version 0.278	0 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources BabySeq Category A gene Expert Review Green Phenotypes Ventricular tachycardia, catecholaminergic polymorphic Arrhythmogenic right ventricular dysplasia 2
Green RYR2 in Incidentalome_PREGEN_DRAFT Version 0.43	0 reviews	Unknown	Sources NSW Health Pathology Expert Review Green
Green RYR2 in BabyScreen+ newborn screening Level 2: Screening Version 1.116	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green BabySeq Category A gene Phenotypes Arrhythmogenic right ventricular dysplasia 2 Ventricular tachycardia, catecholaminergic polymorphic Tags cardiac treatable
Green RYR2 in Transplant Co-Morbidity Superpanel Level 2: Screening Version 0.18	0 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Melbourne Genomics Health Alliance Phenotypes Ventricular tachycardia, catecholaminergic polymorphic, 1, MIM# 604772 Arrhythmogenic right ventricular dysplasia 2 , MIM#600996