COX2, cytochrome c oxidase subunit II, 4513

N. diseases: 875; N. variants: 79
Disease: Mitochondrial Diseases ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1131692064
rs1131692064
Entrez Id: 4508;4509;4513;4514
Gene Symbol: ATP6;ATP8;COX2;COX3
ATP6;ATP8;COX2;COX3
CUI: C0751651
Disease:
Mitochondrial Diseases 		C 0.700 CausalMutation CLINVAR
dbSNP: rs118192098
rs118192098
Entrez Id: 4508;4509;4513;4514;4537;4566
Gene Symbol: ATP6;ATP8;COX2;COX3;ND3;TRNK
ATP6;ATP8;COX2;COX3;ND3;TRNK
CUI: C0751651
Disease:
Mitochondrial Diseases 		G 0.700 CausalMutation CLINVAR