RS118192100 MT-ATP6

Health Risk Chr MT:8362 snv non coding transcript exon variant
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What This Variant Does
"CLNSIG=5
Associated Conditions
Cardiomyopathy and Deafness
Leigh syndrome
MERRF syndrome
MELAS syndrome
Mitochondrial disease
MT-TK-related disorder
Cardiomyopathy and Deafness
Leigh syndrome
MERRF syndrome
MELAS syndrome
Mitochondrial disease
MT-TK-related disorder
Other Variants in MT-ATP6
rs199476133 rs199476135 rs199476138 rs387906423 rs1556423632 rs794726857 rs1569484234 rs1603222000 rs1603221634 rs2521964059
Ask Dr. Hemsworth about this variant