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: rs193922649
rs193922649
Entrez Id: 3920
Gene Symbol: LAMP2
LAMP2
CUI: C0949658
Disease:
Cardiomyopathy, Hypertrophic, Familial 		C 0.700 GeneticVariation CLINVAR