Gene: TRNW ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4578
Gene Symbol: TRNW
TRNW 		0.410 GeneticVariation group BEFREE A novel MT-CO2 m.8249G>A pathogenic variation and the MT-TW m.5521G>A mutation in patients with mitochondrial myopathy. 23841600 2014
Entrez Id: 4578
Gene Symbol: TRNW
TRNW 		0.410 CausalMutation group CLINVAR
Entrez Id: 4578
Gene Symbol: TRNW
TRNW 		0.410 Biomarker group CTD_human
Entrez Id: 4578
Gene Symbol: TRNW
TRNW 		0.410 Biomarker group HPO