Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs387906421
rs387906421
CYTB ; ND6 ; TRNE
C 0.700 GeneticVariation CLINVAR Molecular basis of infantile reversible cytochrome c oxidase deficiency myopathy. 19720722

2009