rs794728924, SCN5A

N. diseases: 1
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 SCN5A variant that blocks fibroblast growth factor homologous factor regulation causes human arrhythmia. 26392562 2015