Disease: Familial (FPAH) ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs199472922
rs199472922
Entrez Id: 3757
Gene Symbol: KCNH2
KCNH2
CUI: C1611743
Disease:
Familial (FPAH) 		0.010 GeneticVariation BEFREE Heterogeneous Phenotype of Long QT Syndrome Caused by the KCNH2-H562R Mutation: Importance of Familial Genetic Testing. 25819988 2015