This test, UGT1A1 Gene Polymorphism (TA Repeat), is used to identify patients with colorectal cancer. Gilbert syndrome and Crigler-Najjar syndromes types I and II are two disorders linked with unconjugated hyperbilirubinemia that can occur from diminished or missing UGT1A1 enzymatic activity caused by genetic variations in the enzyme. The most frequent inherited cause of elevated bilirubin is Gilbert syndrome. Additionally, this test aids in identifying those people who are more likely to experience negative related side effects due to UGT1A1 metabolization.
Sample Type - Blood
Reporting Time - Please Call Customer care
Prerequisites - No special preparation required
Price - ₹9080/-
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