RS187494806 MMACHC

Health Risk Chr 1:45509132
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Associated Conditions
Inborn genetic diseases
Cobalamin C disease
Inborn genetic diseases
Cobalamin C disease
Other Variants in MMACHC
rs398124292 rs121918240 rs121918241 rs121918242 rs121918243 rs587776889 rs370596113 rs1305170860 rs398124294 rs398124295
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