RS143747297 MTO1
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency
Mitochondrial oxidative phosphorylation disorder
Global developmental delay
Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency
Mitochondrial oxidative phosphorylation disorder
Global developmental delay
Other Variants in MTO1