Gene: SCN5A ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1417036453
rs1417036453
SCN5A
A 0.700 CausalMutation CLINVAR

dbSNP: rs727504801
rs727504801
SCN5A
C 0.700 CausalMutation CLINVAR

dbSNP: rs1805124
rs1805124
SCN5A
0.010 GeneticVariation BEFREE Our results showed that the rs1805124 polymorphism was significantly associated with DCM, and the association was more significant in patients with FDC; furthermore, in these individuals, the less frequent GG genotype was associated with a 7.39-fold increased risk of disease [95% confidence interval (95% CI) = 2.88-18.96; P < 0.0001] compared with the AA genotype. 29782370

2018
dbSNP: rs45546039
rs45546039
SCN5A
0.010 GeneticVariation BEFREE Rapid and effective response of the R222Q SCN5A to quinidine treatment in a patient with Purkinje-related ventricular arrhythmia and familial dilated cardiomyopathy: a case report. 29871609

2018