RS200483477 MMACHC

Health Risk Chr 1:45507455
Upload your DNA to see your genotype for this variant.
Associated Conditions
Cobalamin C disease
Disorders of Intracellular Cobalamin Metabolism
Methylmalonic aciduria
type cblc
Inborn genetic diseases
MMACHC-related disorder
Cobalamin C disease
Disorders of Intracellular Cobalamin Metabolism
Methylmalonic aciduria
type cblc
Inborn genetic diseases
MMACHC-related disorder
Other Variants in MMACHC
rs398124292 rs121918240 rs121918241 rs121918242 rs121918243 rs587776889 rs370596113 rs1305170860 rs398124294 rs398124295
Ask Dr. Hemsworth about this variant