RS121913578 MTR
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What This Variant Does
"[OMIM:?]
Associated Conditions
Methylcobalamin deficiency type cblG
Profound intellectual disability
Epilepsy
Inborn genetic diseases
Disorders of Intracellular Cobalamin Metabolism
Homocystinuria
Decreased methionine synthase activity
MTR-related disorder
Methylcobalamin deficiency type cblG
Profound intellectual disability
Epilepsy
Inborn genetic diseases
Disorders of Intracellular Cobalamin Metabolism
Homocystinuria
Decreased methionine synthase activity
Other Variants in MTR