RYR2 Chromosome 1

Ryanodine receptor 2
853 variants 853 Health Risk

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What This Gene Does
This gene encodes a ryanodine receptor found in cardiac muscle sarcoplasmic reticulum. The encoded protein is one of the components of a calcium channel, composed of a tetramer of the ryanodine receptor proteins and a tetramer of FK506 binding protein 1B proteins, that supplies calcium to cardiac muscle. Mutations in this gene are associated with stress-induced polymorphic ventricular tachycardia and arrhythmogenic right ventricular dysplasia. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
"Ryanodine receptors|EF-hand domain containing|Armadillo like helical domain containing|MicroRNA protein coding host genes"
Locus Type
gene with protein product
Location
1q43
Ensembl
ENSG00000198626
Associated Conditions (35)
Cardiomyopathy
Catecholaminergic polymorphic ventricular tachycardia 1
Arrhythmogenic right ventricular dysplasia 2
Ventricular arrhythmias due to cardiac ryanodine receptor calcium release deficiency syndrome
Cardiovascular phenotype
Catecholaminergic polymorphic ventricular tachycardia
RYR2-related disorder
Long QT syndrome
Conduction disorder of the heart
6 conditions
Ventricular fibrillation
paroxysmal familial
type 1
Primary dilated cardiomyopathy
Cardiac arrhythmia
Arrhythmogenic right ventricular dysplasia 9
Wolff-Parkinson-White pattern
Death in infancy
Sudden cardiac death
Hypertrophic cardiomyopathy
+15 more conditions
Key Variants
RS1002006336
Conflicting classifications of pathogenicity
Cardiomyopathy, Catecholaminergic polymorphic ventricular tachycardia 1, Cardiomyopathy
Health Risk
RS1006109370
Conflicting classifications of pathogenicity
Arrhythmogenic right ventricular dysplasia 2, Catecholaminergic polymorphic ventricular tachycardia 1, Ventricular arrhythmias due to cardiac ryanodine receptor calcium release deficiency syndrome
Health Risk
RS1008000319
Conflicting classifications of pathogenicity
Catecholaminergic polymorphic ventricular tachycardia 1, Catecholaminergic polymorphic ventricular tachycardia 1
Health Risk
RS1014182598
Conflicting classifications of pathogenicity
Cardiomyopathy, Catecholaminergic polymorphic ventricular tachycardia 1, Catecholaminergic polymorphic ventricular tachycardia
Health Risk
RS1019112544
Conflicting classifications of pathogenicity
Catecholaminergic polymorphic ventricular tachycardia 1, Arrhythmogenic right ventricular dysplasia 2, Cardiovascular phenotype
Health Risk
RS1024126701
Conflicting classifications of pathogenicity
Cardiomyopathy, Cardiovascular phenotype, Catecholaminergic polymorphic ventricular tachycardia 1
Health Risk
RS1025023837
Conflicting classifications of pathogenicity
Cardiovascular phenotype, Catecholaminergic polymorphic ventricular tachycardia 1, Cardiomyopathy
Health Risk
RS1029442866
Conflicting classifications of pathogenicity
Cardiomyopathy, Catecholaminergic polymorphic ventricular tachycardia 1, Cardiovascular phenotype
Health Risk
RS1032783973
Conflicting classifications of pathogenicity
Cardiomyopathy, Cardiovascular phenotype, Catecholaminergic polymorphic ventricular tachycardia 1
Health Risk
RS1037732490
Conflicting classifications of pathogenicity
Cardiovascular phenotype, Catecholaminergic polymorphic ventricular tachycardia 1, Catecholaminergic polymorphic ventricular tachycardia
Health Risk
RS1042196921
Conflicting classifications of pathogenicity
Cardiomyopathy, Catecholaminergic polymorphic ventricular tachycardia 1, Cardiomyopathy
Health Risk
RS1057521205
Conflicting classifications of pathogenicity
Catecholaminergic polymorphic ventricular tachycardia 1, Arrhythmogenic right ventricular dysplasia 2, Cardiomyopathy
Health Risk
All Variants (853)
RSID Category Clinical Significance Conditions
RS1695358851 Health Risk Conflicting classifications of pathogenicity Catecholaminergic polymorphic ventricular tachycardia 1, Catecholaminergic polymorphic ventricular tachycardia 1
RS1700027349 Health Risk Conflicting classifications of pathogenicity Cardiomyopathy, Catecholaminergic polymorphic ventricular tachycardia 1, Cardiomyopathy
RS1702097862 Health Risk Conflicting classifications of pathogenicity Cardiomyopathy, Catecholaminergic polymorphic ventricular tachycardia 1, Cardiomyopathy
RS180711819 Health Risk Conflicting classifications of pathogenicity Arrhythmogenic right ventricular dysplasia 2, Catecholaminergic polymorphic ventricular tachycardia 1, Catecholaminergic polymorphic ventricular tachycardia
RS182778119 Health Risk Conflicting classifications of pathogenicity Cardiomyopathy, Cardiovascular phenotype, Catecholaminergic polymorphic ventricular tachycardia 1
RS183933829 Health Risk Conflicting classifications of pathogenicity Arrhythmogenic right ventricular dysplasia 2, Catecholaminergic polymorphic ventricular tachycardia 1, Cardiomyopathy
RS184537159 Health Risk Conflicting classifications of pathogenicity Catecholaminergic polymorphic ventricular tachycardia 1, Arrhythmogenic right ventricular dysplasia 2, Catecholaminergic polymorphic ventricular tachycardia 1
RS184625125 Health Risk Conflicting classifications of pathogenicity Catecholaminergic polymorphic ventricular tachycardia 1, Arrhythmogenic right ventricular dysplasia 2, Cardiomyopathy
RS184937795 Health Risk Conflicting classifications of pathogenicity Catecholaminergic polymorphic ventricular tachycardia 1, Arrhythmogenic right ventricular dysplasia 2, Cardiomyopathy
RS185237690 Health Risk Conflicting classifications of pathogenicity Catecholaminergic polymorphic ventricular tachycardia 1, Cardiovascular phenotype, Cardiomyopathy
RS185482345 Health Risk Conflicting classifications of pathogenicity Cardiomyopathy, Catecholaminergic polymorphic ventricular tachycardia 1, Arrhythmogenic right ventricular dysplasia 2
RS185715460 Health Risk Conflicting classifications of pathogenicity Cardiomyopathy, Catecholaminergic polymorphic ventricular tachycardia 1, Cardiovascular phenotype
RS186181155 Health Risk Conflicting classifications of pathogenicity Arrhythmogenic right ventricular dysplasia 2, Cardiovascular phenotype, Cardiomyopathy
RS186326951 Health Risk Conflicting classifications of pathogenicity Arrhythmogenic right ventricular dysplasia 2, Cardiomyopathy, Catecholaminergic polymorphic ventricular tachycardia 1
RS186906598 Health Risk Conflicting classifications of pathogenicity Catecholaminergic polymorphic ventricular tachycardia 1, Cardiovascular phenotype, Cardiomyopathy
RS187977513 Health Risk Conflicting classifications of pathogenicity 6 conditions, Cardiomyopathy, Catecholaminergic polymorphic ventricular tachycardia 1
RS188671846 Health Risk Conflicting classifications of pathogenicity Cardiovascular phenotype, Cardiomyopathy, Catecholaminergic polymorphic ventricular tachycardia 1
RS189772599 Health Risk Conflicting classifications of pathogenicity Catecholaminergic polymorphic ventricular tachycardia, Cardiovascular phenotype, Catecholaminergic polymorphic ventricular tachycardia 1
RS190009333 Health Risk Conflicting classifications of pathogenicity Cardiomyopathy, Cardiovascular phenotype, Catecholaminergic polymorphic ventricular tachycardia 1
RS191850147 Health Risk Conflicting classifications of pathogenicity Cardiomyopathy, Cardiovascular phenotype, Catecholaminergic polymorphic ventricular tachycardia 1
RS192890834 Health Risk Conflicting classifications of pathogenicity Cardiomyopathy, Catecholaminergic polymorphic ventricular tachycardia 1, Catecholaminergic polymorphic ventricular tachycardia
RS193125030 Health Risk Conflicting classifications of pathogenicity Catecholaminergic polymorphic ventricular tachycardia 1, Catecholaminergic polymorphic ventricular tachycardia, Cardiovascular phenotype
RS193922623 Health Risk Conflicting classifications of pathogenicity Ventricular fibrillation, paroxysmal familial, type 1
RS193922624 Health Risk Conflicting classifications of pathogenicity Primary dilated cardiomyopathy, Cardiovascular phenotype, Cardiomyopathy
RS193922625 Health Risk Conflicting classifications of pathogenicity Cardiomyopathy, Cardiac arrhythmia, Cardiomyopathy
RS193922626 Health Risk Conflicting classifications of pathogenicity Cardiomyopathy, Arrhythmogenic right ventricular dysplasia 2, Catecholaminergic polymorphic ventricular tachycardia 1
RS193922628 Health Risk Conflicting classifications of pathogenicity Arrhythmogenic right ventricular dysplasia 2, Cardiovascular phenotype, Cardiomyopathy
RS199624074 Health Risk Conflicting classifications of pathogenicity Cardiomyopathy, Cardiovascular phenotype, Catecholaminergic polymorphic ventricular tachycardia 1
RS199682282 Health Risk Conflicting classifications of pathogenicity Cardiomyopathy, Cardiovascular phenotype, Catecholaminergic polymorphic ventricular tachycardia 1
RS199730192 Health Risk Conflicting classifications of pathogenicity Cardiomyopathy, Arrhythmogenic right ventricular dysplasia 2, Catecholaminergic polymorphic ventricular tachycardia 1
RS199821105 Health Risk Conflicting classifications of pathogenicity Arrhythmogenic right ventricular dysplasia 2, Catecholaminergic polymorphic ventricular tachycardia 1, Cardiomyopathy
RS199893812 Health Risk Conflicting classifications of pathogenicity Catecholaminergic polymorphic ventricular tachycardia, Cardiomyopathy, Cardiovascular phenotype
RS200070226 Health Risk Conflicting classifications of pathogenicity Wolff-Parkinson-White pattern, Cardiomyopathy, Catecholaminergic polymorphic ventricular tachycardia 1
RS200092869 Health Risk Conflicting classifications of pathogenicity Cardiovascular phenotype, Cardiomyopathy, Arrhythmogenic right ventricular dysplasia 2
RS200105499 Health Risk Conflicting classifications of pathogenicity Cardiovascular phenotype, Cardiomyopathy, Catecholaminergic polymorphic ventricular tachycardia 1
RS200121281 Health Risk Conflicting classifications of pathogenicity Long QT syndrome, Cardiomyopathy, Cardiovascular phenotype
RS200197527 Health Risk Conflicting classifications of pathogenicity Cardiomyopathy, Cardiovascular phenotype, Catecholaminergic polymorphic ventricular tachycardia
RS200236750 Health Risk Conflicting classifications of pathogenicity Catecholaminergic polymorphic ventricular tachycardia 1, Death in infancy, Cardiovascular phenotype
RS200318013 Health Risk Conflicting classifications of pathogenicity Conduction disorder of the heart, Cardiomyopathy, Cardiovascular phenotype
RS200420897 Health Risk Conflicting classifications of pathogenicity Primary dilated cardiomyopathy, Cardiovascular phenotype, Cardiomyopathy
RS200450676 Health Risk Conflicting classifications of pathogenicity Catecholaminergic polymorphic ventricular tachycardia 1, Arrhythmogenic right ventricular dysplasia 2, Long QT syndrome
RS200525962 Health Risk Conflicting classifications of pathogenicity Sudden cardiac death, Cardiomyopathy, Arrhythmogenic right ventricular dysplasia 2
RS200574919 Health Risk Conflicting classifications of pathogenicity Cardiomyopathy, Cardiovascular phenotype, Arrhythmogenic right ventricular dysplasia 2
RS200642525 Health Risk Conflicting classifications of pathogenicity Arrhythmogenic right ventricular dysplasia 2, Cardiovascular phenotype, Catecholaminergic polymorphic ventricular tachycardia 1
RS200803276 Health Risk Conflicting classifications of pathogenicity Cardiomyopathy, Cardiovascular phenotype, Arrhythmogenic right ventricular dysplasia 2
RS201079716 Health Risk Conflicting classifications of pathogenicity Catecholaminergic polymorphic ventricular tachycardia 1, Arrhythmogenic right ventricular dysplasia 2, Cardiomyopathy
RS201131315 Health Risk Conflicting classifications of pathogenicity Cardiovascular phenotype, Cardiomyopathy, Catecholaminergic polymorphic ventricular tachycardia 1
RS201218861 Health Risk Conflicting classifications of pathogenicity Catecholaminergic polymorphic ventricular tachycardia 1, Arrhythmogenic right ventricular dysplasia 2, Cardiomyopathy
RS201312753 Health Risk Conflicting classifications of pathogenicity Cardiomyopathy, Cardiovascular phenotype, Arrhythmogenic right ventricular dysplasia 2
RS201371633 Health Risk Conflicting classifications of pathogenicity Catecholaminergic polymorphic ventricular tachycardia, Cardiovascular phenotype, Cardiomyopathy
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