RS199730889 TRMT10C
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What This Variant Does
"CLNSIG=5
Associated Conditions
Combined oxidative phosphorylation defect type 30
Mitochondrial disease
See cases
TRMT10C-related disorder
Combined oxidative phosphorylation defect type 30
Mitochondrial disease
See cases
TRMT10C-related disorder
Other Variants in TRMT10C