Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs41261344
rs41261344
SCN5A
0.030 GeneticVariation BEFREE <b>Conclusion:</b> A common SCN5A polymorphism R1193Q enhances UDB by propafenone and predisposes the patients to drug-induced BrS with PIP treatment. 30984031

2019
dbSNP: rs41261344
rs41261344
SCN5A
0.030 GeneticVariation BEFREE SCN5A(R1193Q) is often identified in patients with type 3 long QT syndrome and Brugada syndrome. 30419068

2018
dbSNP: rs41261344
rs41261344
SCN5A
0.030 GeneticVariation BEFREE DNA analysis revealed a missense mutation (R1193Q) in the SCN5A gene, previously linked with familial sudden unexpected nocturnal death syndrome, also known as Brugada syndrome. 15851440

2005