RS201182814 MOCS2

Health Risk Chr 5:53107130
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Associated Conditions
Inborn genetic diseases
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B
Inborn genetic diseases
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B
Other Variants in MOCS2
rs398122797 rs121908605 rs398122798 rs398122799 rs121908606 rs121908607 rs121908608 rs121908609 rs397518417 rs2233218
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