Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs199476104
rs199476104
CYTB ; ND5 ; ND6
C 0.700 CausalMutation CLINVAR Leigh-like encephalopathy complicating Leber's hereditary optic neuropathy. 12205655

2002