rs794728865, SCN5A

N. diseases: 2
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Brugada Syndrome (disorder)
CUI: C1142166
Disease: Brugada Syndrome (disorder)
0.700 CausalMutation CLINVAR Brugada syndrome 2012. 22789973 2012
Brugada Syndrome (disorder)
CUI: C1142166
Disease: Brugada Syndrome (disorder)
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
Romano-Ward Syndrome
CUI: C0035828
Disease: Romano-Ward Syndrome
0.700 GeneticVariation CLINVAR