Disease: Syncope ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7626962
rs7626962
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C0039070
Disease:
Syncope 		0.010 GeneticVariation BEFREE Our study shows that mutation S1103Y does exist in the white population, and it is associated with a considerable risk of syncope, ventricular arrhythmia, ventricular fibrillation, and sudden death in this population. 12471205 2002