RS79457258 RYR2

Health Risk Chr 1:237550629
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Cardiomyopathy
Catecholaminergic polymorphic ventricular tachycardia 1
Catecholaminergic polymorphic ventricular tachycardia
Cardiovascular phenotype
Ventricular arrhythmias due to cardiac ryanodine receptor calcium release deficiency syndrome
Cardiomyopathy
Catecholaminergic polymorphic ventricular tachycardia 1
Catecholaminergic polymorphic ventricular tachycardia
Cardiovascular phenotype
Ventricular arrhythmias due to cardiac ryanodine receptor calcium release deficiency syndrome
Other Variants in RYR2
rs121918597 rs121918598 rs121918599 rs121918600 rs121918601 rs121918602 rs121918603 rs121918604 rs121918605 rs193922622
Ask Dr. Hemsworth about this variant