Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs199472730
rs199472730
KCNQ1
0.710 GeneticVariation BEFREE The inconsistent association of the KCNQ1 S277L mutation with the clinical presentation suggests that additional genetic, epigenetic, or environmental factors play a role in defining the individual clinical LQTS phenotype. 21241800

2011
dbSNP: rs199472730
rs199472730
KCNQ1
T 0.710 CausalMutation CLINVAR

dbSNP: rs199472730
rs199472730
KCNQ1
G 0.710 GeneticVariation CLINVAR