Disease: Syncope ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs199473103
rs199473103
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
CUI: C0039070
Disease:
Syncope 		0.010 GeneticVariation BEFREE A missense mutation (A390V-SNTA1) was found in a patient with recurrent syncope and markedly prolonged QT interval (QTc, 530 ms). 18591664 2008