RS2114693876 NUS1

Health Risk Chr 6:117703603
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Associated Conditions
Intellectual disability
autosomal dominant 55
with seizures
Congenital disorder of glycosylation
type IAA
Intellectual disability
autosomal dominant 55
with seizures
Congenital disorder of glycosylation
type IAA
Other Variants in NUS1
rs886037858 rs1554202698 rs1554200722 rs150646335 rs1582461023 rs146171115 rs1582477100 rs1582461267 rs1582461235 rs1772963498
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