RS200236750 RYR2

Health Risk Chr 1:237566672
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What This Variant Does
"CLNSIG=5
Associated Conditions
Catecholaminergic polymorphic ventricular tachycardia 1
Death in infancy
Cardiovascular phenotype
Cardiomyopathy
RYR2-related disorder
Catecholaminergic polymorphic ventricular tachycardia 1
Death in infancy
Cardiovascular phenotype
Cardiomyopathy
RYR2-related disorder
Other Variants in RYR2
rs121918597 rs121918598 rs121918599 rs121918600 rs121918601 rs121918602 rs121918603 rs121918604 rs121918605 rs193922622
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