RS121908987 PRKAG2
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What This Variant Does
"The rare minor allele of this variant is reported to be pathogenic/likely pathogenic for familial hy...
Associated Conditions
Wolff-Parkinson-White pattern
Hypertrophic cardiomyopathy 6
Primary familial hypertrophic cardiomyopathy
Lethal congenital glycogen storage disease of heart
Cardiovascular phenotype
Cardiomyopathy
Hypertrophic cardiomyopathy
Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome
Lethal congenital glycogen storage disease of heart
Cardiovascular phenotype
Wolff-Parkinson-White pattern
Hypertrophic cardiomyopathy 6
Primary familial hypertrophic cardiomyopathy
Lethal congenital glycogen storage disease of heart
Cardiovascular phenotype
Other Variants in PRKAG2