RS138081800 UPB1

Health Risk Chr 22:24500104 snv splice acceptor variant
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What This Variant Does
"CLNSIG=5
Associated Conditions
Deficiency of beta-ureidopropionase
Inborn genetic diseases
UPB1-related disorder
Deficiency of beta-ureidopropionase
Inborn genetic diseases
UPB1-related disorder
Population Frequencies
gnomAD ALL
0%
Other Variants in UPB1
rs34035085 rs118163237 rs747539101 rs145749836 rs200161281 rs199788632 rs770091394 rs200145797 rs143493067 rs145766755
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