RS80338677 MAN2B1

Health Risk Chr 19:12655693
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What This Variant Does
"CLNSIG=5
Associated Conditions
Deficiency of alpha-mannosidase
Inborn genetic diseases
Ovarian serous cystadenocarcinoma
Deficiency of alpha-mannosidase
Inborn genetic diseases
Ovarian serous cystadenocarcinoma
Other Variants in MAN2B1
rs387906261 rs121434331 rs121434332 rs80338680 rs121434333 rs80338678 rs80338679 rs80338681 rs398123455 rs398123456
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