Gene: KCNQ1 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs120074187
rs120074187
KCNQ1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs201698592
rs201698592
KCNQ1 ; KCNQ1-AS1
0.010 GeneticVariation BEFREE Moreover, 2 rare variants (KCNQ1: c.1944C>T and SCN5A: c.3621C>T) showed an elevated allelic frequency (more than 1.5-fold) in the AMI_VA group when compared to the AMI group. 31751991

2020
dbSNP: rs120074192
rs120074192
KCNQ1
0.010 GeneticVariation BEFREE In addition, the KCNQ1 S140G mutation can induce ventricular arrhythmia and lessen ventricular contractility under re-entrant conditions. 30108508

2018