RS2114696019 NUS1

Health Risk Chr 6:117707001
Upload your DNA to see your genotype for this variant.
Associated Conditions
Congenital disorder of glycosylation
type IAA
NUS1-related epilepsy-myoclonus-ataxia syndrome
Congenital disorder of glycosylation
type IAA
NUS1-related epilepsy-myoclonus-ataxia syndrome
Other Variants in NUS1
rs886037858 rs1554202698 rs1554200722 rs150646335 rs1582461023 rs146171115 rs1582477100 rs1582461267 rs1582461235 rs1772963498
Ask Dr. Hemsworth about this variant