Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs199472924
rs199472924
KCNH2
0.710 GeneticVariation BEFREE The distinct HERG missense mutation L564P causes long QT syndrome in one French Canadian family. 10744792

2000
dbSNP: rs199472924
rs199472924
KCNH2
T 0.710 GeneticVariation CLINVAR