Gene: CYTB ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4519
Gene Symbol: CYTB
CYTB 		0.110 GeneticVariation disease BEFREE Mitochondrial encephalomyopathy and complex III deficiency associated with a stop-codon mutation in the cytochrome b gene. 11047755 2000
Entrez Id: 4519
Gene Symbol: CYTB
CYTB 		0.110 CausalMutation disease CLINVAR