Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1805123
rs1805123
KCNH2
0.020 GeneticVariation BEFREE Our findings suggest that K897T may contribute to the occurrence of syncope. 28336205

2017
dbSNP: rs1805123
rs1805123
KCNH2
0.020 GeneticVariation BEFREE Subgroup analysis showed that the presence of the K897T polymorphism in the LQT2 gene in an affected family was associated with an 11-fold (P=0.001) increase in the risk of recurrent syncope in genotype-negative subjects. 21831960

2011