rs207459999, CYTB;ND6

N. diseases: 2
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Leigh Disease
CUI: C0023264
Disease: Leigh Disease
0.700 CausalMutation CLINVAR Mitochondrial encephalomyopathy and complex III deficiency associated with a stop-codon mutation in the cytochrome b gene. 11047755 2000
Mitochondrial Encephalomyopathies
CUI: C0162666
Disease: Mitochondrial Encephalomyopathies
0.700 CausalMutation CLINVAR