Disease: Syncope ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs566251672
rs566251672
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C0039070
Disease:
Syncope 		0.010 GeneticVariation BEFREE A Caucasian family with syncope and marginally prolonged QT interval was screened for LQTS-susceptibility genes and found to harbor the R800L mutation in SCN5A and A261V mutation in SNTA1, and those with both mutations had the strongest clinical phenotype. 23376825 2013