RS1603222000 MT-ATP6

Health Risk Chr MT:9035
Upload your DNA to see your genotype for this variant.
Associated Conditions
Progressive cerebellar ataxia
Leigh syndrome
See cases
Leber optic atrophy
Mitochondrial disease
MT-ATP6-related primary mitochondrial disease
MT-ATP6-related disorder
NARP syndrome
Primary mitochondrial disorders
Progressive cerebellar ataxia
Leigh syndrome
See cases
Leber optic atrophy
Mitochondrial disease
MT-ATP6-related primary mitochondrial disease
Other Variants in MT-ATP6
rs199476133 rs199476135 rs199476138 rs387906423 rs1556423632 rs794726857 rs1569484234 rs1603221634 rs2521964059
Ask Dr. Hemsworth about this variant