RS193922623 RYR2

Health Risk Chr 1:237500774
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What This Variant Does
"CLNSIG=4
Associated Conditions
Ventricular fibrillation
paroxysmal familial
type 1
Arrhythmogenic right ventricular dysplasia 2
Cardiovascular phenotype
Catecholaminergic polymorphic ventricular tachycardia 1
Cardiomyopathy
Ventricular fibrillation
paroxysmal familial
type 1
Arrhythmogenic right ventricular dysplasia 2
Cardiovascular phenotype
Catecholaminergic polymorphic ventricular tachycardia 1
Cardiomyopathy
Other Variants in RYR2
rs121918597 rs121918598 rs121918599 rs121918600 rs121918601 rs121918602 rs121918603 rs121918604 rs121918605 rs193922622
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