rs1047624774, ATP2B4

N. diseases: 2
Disease: Syncope ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Syncope
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