RS199476135 MT-ATP6
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Leigh syndrome
Striatonigral degeneration
infantile
mitochondrial
Mitochondrial complex 5 (ATP synthase) deficiency
mitochondrial type 1
Leber optic atrophy
Maternally-inherited spastic paraplegia
Mitochondrial disease
NARP syndrome
MT-ATP6-related disorder
Primary mitochondrial disorders
Leigh syndrome
Mitochondrial complex 5 (ATP synthase) deficiency
mitochondrial type 1
Other Variants in MT-ATP6