Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121912512
rs121912512
KCNH2
0.710 GeneticVariation BEFREE Direct bidirectional sequencing of long QT syndrome genes identified a previously unreported HERG missense mutation (R752Q). 12621127

2003
dbSNP: rs121912512
rs121912512
KCNH2
T 0.710 GeneticVariation CLINVAR