RS759244819 ALG12

Health Risk Chr 22:49904498
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What This Variant Does
"CLNSIG=5
Associated Conditions
ALG12-congenital disorder of glycosylation
Inborn genetic diseases
ALG12-congenital disorder of glycosylation
Inborn genetic diseases
Other Variants in ALG12
rs28942090 rs121907931 rs121907932 rs121907933 rs121907934 rs121907935 rs113652023 rs761221480 rs375721419 rs140835842
Ask Dr. Hemsworth about this variant