Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs730880404
rs730880404
ACTC1 ; LOC101928174
A 0.700 GeneticVariation CLINVAR Advanced heart failure with preserved systolic function in nonobstructive hypertrophic cardiomyopathy: under-recognized subset of candidates for heart transplant. 25239116

2014
dbSNP: rs730880404
rs730880404
ACTC1 ; LOC101928174
A 0.700 GeneticVariation CLINVAR Double or compound sarcomere mutations in hypertrophic cardiomyopathy: a potential link to sudden death in the absence of conventional risk factors. 21839045

2012
dbSNP: rs730880404
rs730880404
ACTC1 ; LOC101928174
A 0.700 GeneticVariation CLINVAR Prevalence and clinical profile of myocardial crypts in hypertrophic cardiomyopathy. 22563033

2012