Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs199473479
rs199473479
KCNQ1
0.710 GeneticVariation BEFREE We identified the missense mutation M520R in the calmodulin binding domain of the Kv7.1 channel from a German family with long QT-syndrome. 17482572

2007
dbSNP: rs199473479
rs199473479
KCNQ1
G 0.710 CausalMutation CLINVAR