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: rs121434475
rs121434475
Entrez Id: 4514;4537;4538;4539;4563
Gene Symbol: COX3;ND3;ND4;ND4L;TRNG
COX3;ND3;ND4;ND4L;TRNG
CUI: C0949658
Disease:
Cardiomyopathy, Hypertrophic, Familial 		C 0.700 CausalMutation CLINVAR