RS187089611 UNC80

Health Risk Chr 2:209877990
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
Hypotonia
infantile
with psychomotor retardation and characteristic facies 2
Inborn genetic diseases
Hypotonia
infantile
with psychomotor retardation and characteristic facies 2
Other Variants in UNC80
rs864321623 rs200659479 rs864321622 rs869025316 rs869025317 rs869025318 rs869025319 rs869025320 rs200473652 rs886041094
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