Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1064795333
rs1064795333
KCNQ1
0.710 GeneticVariation BEFREE Mutations in Danish patients with long QT syndrome and the identification of a large founder family with p.F29L in KCNH2. 24606995

2014
dbSNP: rs1064795333
rs1064795333
KCNQ1
A 0.710 CausalMutation CLINVAR