RS769648248 PMM2

Health Risk Chr 16:8804793
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
PMM2-congenital disorder of glycosylation
Inborn genetic diseases
PMM2-congenital disorder of glycosylation
PMM2-congenital disorder of glycosylation
Inborn genetic diseases
PMM2-congenital disorder of glycosylation
Other Variants in PMM2
rs2060938199 rs28936415 rs78290141 rs104894525 rs104894526 rs104894527 rs80338701 rs80338704 rs104894530 rs104894531
Ask Dr. Hemsworth about this variant