RS61736440 MTR

Health Risk Chr 1:236852997
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Associated Conditions
Methylcobalamin deficiency type cblG
Neural tube defects
folate-sensitive
Disorders of Intracellular Cobalamin Metabolism
Inborn genetic diseases
Methylcobalamin deficiency type cblG
Neural tube defects
folate-sensitive
Disorders of Intracellular Cobalamin Metabolism
Inborn genetic diseases
Other Variants in MTR
rs121913578 rs121913579 rs1661117141 rs797044444 rs797044445 rs121913580 rs121913581 rs121913582 rs794727395 rs116836001
Ask Dr. Hemsworth about this variant