RS2512503266 MAN2B1

Health Risk Chr 19:12658147
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Associated Conditions
Inborn genetic diseases
Deficiency of alpha-mannosidase
Inborn genetic diseases
Deficiency of alpha-mannosidase
Other Variants in MAN2B1
rs387906261 rs121434331 rs121434332 rs80338680 rs121434333 rs80338677 rs80338678 rs80338679 rs80338681 rs398123455
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