Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs199472712
rs199472712
KCNQ1
T 0.700 GeneticVariation CLINVAR Cellular mechanisms of mutations in Kv7.1: auditory functions in Jervell and Lange-Nielsen syndrome vs. Romano-Ward syndrome. 25705178

2015
dbSNP: rs199472712
rs199472712
KCNQ1
T 0.700 GeneticVariation CLINVAR Mutations in conserved amino acids in the KCNQ1 channel and risk of cardiac events in type-1 long-QT syndrome. 19490272

2009
dbSNP: rs199472712
rs199472712
KCNQ1
T 0.700 GeneticVariation CLINVAR Genomic organization and mutational analysis of KVLQT1, a gene responsible for familial long QT syndrome. 9799083

1998
dbSNP: rs199472712
rs199472712
KCNQ1
A 0.700 GeneticVariation CLINVAR