RS201675951 RYR2
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Primary dilated cardiomyopathy
Primary familial hypertrophic cardiomyopathy
Cardiomyopathy
Catecholaminergic polymorphic ventricular tachycardia 1
Catecholaminergic polymorphic ventricular tachycardia
Primary dilated cardiomyopathy
Primary familial hypertrophic cardiomyopathy
Cardiomyopathy
Catecholaminergic polymorphic ventricular tachycardia 1
Catecholaminergic polymorphic ventricular tachycardia
Other Variants in RYR2