Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267606978
rs267606978
PRKAG2
G 0.700 GeneticVariation CLINVAR Severe hypertrophic cardiomyopathy in an infant with a novel PRKAG2 gene mutation: potential differences between infantile and adult onset presentation. 19787389

2009
dbSNP: rs267606978
rs267606978
PRKAG2
G 0.700 GeneticVariation CLINVAR Ventricular pre-excitation and cardiac hypertrophy mimicking hypertrophic cardiomyopathy in a Turkish family with a novel PRKAG2 mutation. 16716659

2006