RS148041351 CP

Health Risk Chr 3:149212544
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Associated Conditions
Deficiency of ferroxidase
Inborn genetic diseases
Deficiency of ferroxidase
Inborn genetic diseases
Other Variants in CP
rs386134142 rs386134149 rs386134145 rs121909579 rs386134143 rs386134127 rs200683433 rs386134125 rs386134129 rs386134131
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