RS536000212 TRIT1
Upload your DNA to see your genotype for this variant.
Associated Conditions
Epileptic encephalopathy
See cases
TRIT1 Deficiency
Combined oxidative phosphorylation deficiency 35
Epileptic encephalopathy
See cases
TRIT1 Deficiency
Combined oxidative phosphorylation deficiency 35
Other Variants in TRIT1