TRNW, tRNA, 4578

N. diseases: 188; N. variants: 7
Disease: Mitochondrial Myopathies ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs199474673
rs199474673
Entrez Id: 4512;4536;4578
Gene Symbol: COX1;ND2;TRNW
COX1;ND2;TRNW
CUI: C0162670
Disease:
Mitochondrial Myopathies 		A 0.700 CausalMutation CLINVAR