RS121913013 DSG2

Health Risk Chr 18:31519887
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What This Variant Does
"[OMIM:?]
Associated Conditions
Arrhythmogenic right ventricular dysplasia 10
Dilated cardiomyopathy 1BB
Arrhythmogenic right ventricular cardiomyopathy
Primary familial hypertrophic cardiomyopathy
Catecholaminergic polymorphic ventricular tachycardia 1
Cardiovascular phenotype
Cardiomyopathy
Long QT syndrome
DSG2-related disorder
Arrhythmogenic right ventricular dysplasia 10
Dilated cardiomyopathy 1BB
Arrhythmogenic right ventricular cardiomyopathy
Primary familial hypertrophic cardiomyopathy
Catecholaminergic polymorphic ventricular tachycardia 1
Cardiovascular phenotype
Other Variants in DSG2
rs121913006 rs121913007 rs121913008 rs121913010 rs121913011 rs397514038 rs193922639 rs2230234 rs397516701 rs200484060
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