RS863224209 SLC25A4
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What This Variant Does
"CLNSIG=5
Associated Conditions
Mitochondrial DNA depletion syndrome 12B (cardiomyopathic type)
autosomal recessive
SLC25A4-related disorder
Progressive external ophthalmoplegia with mitochondrial DNA deletions
autosomal dominant 2
Mitochondrial DNA depletion syndrome 12B (cardiomyopathic type)
autosomal recessive
SLC25A4-related disorder
Progressive external ophthalmoplegia with mitochondrial DNA deletions
autosomal dominant 2
Other Variants in SLC25A4