RS1168827071 TK2

Health Risk Chr 16:66513771
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Associated Conditions
Mitochondrial DNA depletion syndrome
myopathic form
Inborn mitochondrial myopathy
Mitochondrial disease
Progressive external ophthalmoplegia with mitochondrial DNA deletions
autosomal recessive 3
Mitochondrial DNA depletion syndrome
myopathic form
Inborn mitochondrial myopathy
Mitochondrial disease
Progressive external ophthalmoplegia with mitochondrial DNA deletions
autosomal recessive 3
Other Variants in TK2
rs137854429 rs137854430 rs137854431 rs137854432 rs281865500 rs281865486 rs281865503 rs281865504 rs281865499 rs138439950
Ask Dr. Hemsworth about this variant