Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs199472823
rs199472823
KCNQ1
0.010 GeneticVariation BEFREE A novel KCNQ1 variant (L203P) associated with torsades de pointes-related syncope in a Steinert syndrome patient. 21459285

2011