Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs120074195
rs120074195
KCNQ1
0.010 GeneticVariation BEFREE This study further substantiates a causal link between the V307L KCNQ1 mutation and pro-arrhythmia in human ventricles, and establishes partial inhibition of I<sub>Ks</sub> as a potential anti-arrhythmic strategy in SQT2. 28814790

2017