RS138479499 TK2
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What This Variant Does
"CLNSIG=5
Associated Conditions
Mitochondrial DNA depletion syndrome
myopathic form
Progressive external ophthalmoplegia with mitochondrial DNA deletions
autosomal recessive 3
Mitochondrial disease
Mitochondrial DNA depletion syndrome
myopathic form
Progressive external ophthalmoplegia with mitochondrial DNA deletions
autosomal recessive 3
Mitochondrial disease
Other Variants in TK2