RS149678769 MTRR

Health Risk Chr 5:7889130
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Associated Conditions
Disorders of Intracellular Cobalamin Metabolism
Methylcobalamin deficiency type cblE
Inborn genetic diseases
Disorders of Intracellular Cobalamin Metabolism
Methylcobalamin deficiency type cblE
Inborn genetic diseases
Other Variants in MTRR
rs2126812944 rs137853061 rs2126808021 rs137853062 rs796052001 rs148909799 rs147277149 rs368391537 rs202110383 rs753947379
Ask Dr. Hemsworth about this variant