Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs727503253
rs727503253
A 0.700 CausalMutation CLINVAR Genetic Testing in Pediatric Left Ventricular Noncompaction. 29212898

2017

dbSNP: rs727503253
rs727503253
A 0.700 CausalMutation CLINVAR Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples. 27532257

2017

dbSNP: rs727503253
rs727503253
A 0.700 CausalMutation CLINVAR Genetic analysis in 418 index patients with idiopathic dilated cardiomyopathy: overview of 10 years' experience. 23349452

2013

dbSNP: rs727503253
rs727503253
A 0.700 CausalMutation CLINVAR Haplotype sharing test maps genes for familial cardiomyopathies. 20573160

2011

dbSNP: rs727503253
rs727503253
A 0.700 CausalMutation CLINVAR Novel correlations between the genotype and the phenotype of hypertrophic and dilated cardiomyopathy: results from the German Competence Network Heart Failure. 21750094

2011