Gene: SNTA1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6640
Gene Symbol: SNTA1
SNTA1 		0.120 GeneticVariation phenotype 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
Entrez Id: 6640
Gene Symbol: SNTA1
SNTA1 		0.120 GeneticVariation phenotype BEFREE A missense mutation (A390V-SNTA1) was found in a patient with recurrent syncope and markedly prolonged QT interval (QTc, 530 ms). 18591664 2008
Entrez Id: 6640
Gene Symbol: SNTA1
SNTA1 		0.120 Biomarker phenotype HPO