Popular Tests
    Top test not found
Popular Packages
    Top test not found

Popular Tests
    Top test not found
Popular Packages
    Top test not found

App Available On:

Call us at9166 125 555
Test

UGT1A1 GENE POLYMORPHISM (O.S)

MRP: ₹6200

Recommended For

MaleFemale
  • Age Group
    0-99 Years
  • Report Generation Time
    07-Jun-2023 12:47 AM
  • Sample Type
    EDTA Blood
  • Collection At
    HomeLab
Description

Genetic variants in UGT1A1 may cause reduced or absent UGT1A1 enzymatic activity, resulting in conditions associated with unconjugated hyperbilirubinemia including Gilbert syndrome and Crigler-Najjar syndromes types I and II. Gilbert syndrome is the most common hereditary cause of increased bilirubin. This assay also helps in identifying individuals who are at increased risk of adverse reactions with drugs that are metabolized by UGT1A1 including Irinotecan, Atazanavir, Nilotinib, Pazopanib and Belinostat.

Pre-Information

No specific preparation required

You can also add

  • UGT1A1 GENE POLYMORPHISM (O.S)
    1 Test Included

    6200

    Add
  • UGT1A1 GENE POLYMORPHISM (O.S)
    1 Test Included

    6200

    Add
  • UGT1A1 GENE POLYMORPHISM (O.S)
    1 Test Included

    6200

    Add

Dr. B Lal App Available
in Both Platforms.

Dr. B Lal App Available
in Both Platforms.

Download the free health test app from Dr. B. Lal Clinical Laboratory. Find all the healthcare information and needs you require in just one place. You can schedule home collection, see reports, save medical history, search for more than 1800 tests, and more with just one app. Available both on iOS and Android. Simplify healthcare, download the Dr. B. Lal Clinical Lab App.

Download The App Now
© Copyright 2022 - Dr. B. Lal Clinical Laboratory Pvt. Ltd. All Rights Reserved.