RS121912683 SLC25A4
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Mitochondrial DNA depletion syndrome 12B (cardiomyopathic type)
autosomal recessive
Inborn mitochondrial myopathy
Hypertrophic cardiomyopathy
Mitochondrial respiratory chain defects
Abnormality of mitochondrial metabolism
Myopia
Progressive sensorineural hearing impairment
Vertigo
Left ventricular hypertrophy
Progressive external ophthalmoplegia with mitochondrial DNA deletions
autosomal dominant 2
Mitochondrial DNA depletion syndrome 12B (cardiomyopathic type)
autosomal recessive
Inborn mitochondrial myopathy
Other Variants in SLC25A4