Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs120074186
rs120074186
KCNQ1
A 0.700 CausalMutation CLINVAR KCNQ1 mutations in patients with a family history of lethal cardiac arrhythmias and sudden death. 12702160

2003