RS72558416 OTC
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What This Variant Does
"CLNSIG=5
Associated Conditions
Ornithine carbamoyltransferase deficiency
Inborn genetic diseases
Likely inborn error of metabolism
Ornithine carbamoyltransferase deficiency
Inborn genetic diseases
Ornithine carbamoyltransferase deficiency
Inborn genetic diseases
Likely inborn error of metabolism
Ornithine carbamoyltransferase deficiency
Inborn genetic diseases
Other Variants in OTC