RS398123312 PMM2

Health Risk Chr 16:8801827
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What This Variant Does
"CLNSIG=255
Associated Conditions
PMM2-congenital disorder of glycosylation
Inborn genetic diseases
PMM2-related disorder
PMM2-congenital disorder of glycosylation
Inborn genetic diseases
PMM2-related disorder
Other Variants in PMM2
rs2060938199 rs28936415 rs78290141 rs104894525 rs104894526 rs104894527 rs80338701 rs80338704 rs104894530 rs104894531
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