RS140522266 MMACHC

Health Risk Chr 1:45508806
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What This Variant Does
"CLNSIG=5
Associated Conditions
Cobalamin C disease
Disorders of Intracellular Cobalamin Metabolism
Cobalamin C disease
Homocystinuria
Methylmalonic aciduria
Inborn genetic diseases
MMACHC-related disorder
Cobalamin C disease
Disorders of Intracellular Cobalamin Metabolism
Cobalamin C disease
Homocystinuria
Methylmalonic aciduria
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