RS201669522 RYR2

Health Risk Chr 1:237423225
Upload your DNA to see your genotype for this variant.
Associated Conditions
Arrhythmogenic right ventricular dysplasia 2
Wolff-Parkinson-White pattern
Catecholaminergic polymorphic ventricular tachycardia 1
Cardiomyopathy
Ventricular arrhythmias due to cardiac ryanodine receptor calcium release deficiency syndrome
Cardiovascular phenotype
Catecholaminergic polymorphic ventricular tachycardia
Arrhythmogenic right ventricular dysplasia 2
Wolff-Parkinson-White pattern
Catecholaminergic polymorphic ventricular tachycardia 1
Cardiomyopathy
Ventricular arrhythmias due to cardiac ryanodine receptor calcium release deficiency syndrome
Cardiovascular phenotype
Catecholaminergic polymorphic ventricular tachycardia
Other Variants in RYR2
rs121918597 rs121918598 rs121918599 rs121918600 rs121918601 rs121918602 rs121918603 rs121918604 rs121918605 rs193922622
Ask Dr. Hemsworth about this variant