Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs199472709
rs199472709
KCNQ1
A 0.700 CausalMutation CLINVAR UniProt: a hub for protein information. 25348405

2015
dbSNP: rs199472709
rs199472709
KCNQ1
A 0.700 CausalMutation CLINVAR Early repolarization is associated with symptoms in patients with type 1 and type 2 long QT syndrome. 24861447

2014
dbSNP: rs199472709
rs199472709
KCNQ1
A 0.700 CausalMutation CLINVAR A KCNQ1 mutation causes a high penetrance for familial atrial fibrillation. 23350853

2013
dbSNP: rs199472709
rs199472709
KCNQ1
A 0.700 CausalMutation CLINVAR R231C mutation in KCNQ1 causes long QT syndrome type 1 and familial atrial fibrillation. 20850564

2011
dbSNP: rs199472709
rs199472709
KCNQ1
A 0.700 CausalMutation CLINVAR Genetic testing for long-QT syndrome: distinguishing pathogenic mutations from benign variants. 19841300

2009
dbSNP: rs199472709
rs199472709
KCNQ1
A 0.700 CausalMutation CLINVAR Genetic testing in the long QT syndrome: development and validation of an efficient approach to genotyping in clinical practice. 16414944

2005
dbSNP: rs199472709
rs199472709
KCNQ1
A 0.700 CausalMutation CLINVAR Four potassium channel mutations account for 73% of the genetic spectrum underlying long-QT syndrome (LQTS) and provide evidence for a strong founder effect in Finland. 15176425

2004