Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs730880850
rs730880850
MYH7
T 0.700 CausalMutation CLINVAR Prenatal ultrasound diagnosis of MYH7 non-compaction cardiomyopathy. 22859017

2013
dbSNP: rs730880850
rs730880850
MYH7
T 0.700 CausalMutation CLINVAR Interpreting secondary cardiac disease variants in an exome cohort. 23861362

2013
dbSNP: rs730880850
rs730880850
MYH7
T 0.700 CausalMutation CLINVAR Sarcomere gene mutations in isolated left ventricular noncompaction cardiomyopathy do not predict clinical phenotype. 21551322

2011
dbSNP: rs730880850
rs730880850
MYH7
T 0.700 CausalMutation CLINVAR Mutations in sarcomere protein genes in left ventricular noncompaction. 18506004

2008