RS778381859 TCN2

Health Risk Chr 22:30614416
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Transcobalamin II deficiency
Inborn genetic diseases
Transcobalamin II deficiency
Other Variants in TCN2
rs1157135425 rs606231119 rs372866837 rs61748898 rs138738105 rs201408393 rs35997415 rs886057397 rs143250551 rs201344377
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