Disease: Cardiomyopathy, Hypertrophic, Familial ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs199472948
rs199472948
Entrez Id: 3757
Gene Symbol: KCNH2
KCNH2
CUI: C0949658
Disease:
Cardiomyopathy, Hypertrophic, Familial 		T 0.700 GeneticVariation CLINVAR