Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs727504801
rs727504801
SCN5A
C 0.700 CausalMutation CLINVAR Parental electrocardiographic screening identifies a high degree of inheritance for congenital and childhood nonimmune isolated atrioventricular block. 22899775

2012
dbSNP: rs727504801
rs727504801
SCN5A
C 0.700 CausalMutation CLINVAR SCN5A mutations associate with arrhythmic dilated cardiomyopathy and commonly localize to the voltage-sensing mechanism. 21596231

2011
dbSNP: rs727504801
rs727504801
SCN5A
C 0.700 CausalMutation CLINVAR An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing. 20129283

2010
dbSNP: rs727504801
rs727504801
SCN5A
C 0.700 CausalMutation CLINVAR Sodium channel mutations and susceptibility to heart failure and atrial fibrillation. 15671429

2005
dbSNP: rs727504801
rs727504801
SCN5A
C 0.700 CausalMutation CLINVAR Genetic basis and molecular mechanism for idiopathic ventricular fibrillation. 9521325

1998