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DNA Labs India

Liver & Hepatology

DNA Labs India | Diagnostic Tests

Liver & Hepatology

Clinical Overview

Sub-category mapping under Genetics & Genomics

| Reviewed by: Dr. Rajesh Kumar, MD Pathology | ISO 9001:2015 Certified Laboratory

This content is for educational purposes only. Always consult a qualified healthcare provider for medical advice.

Tests

Interleukin 28B rs12979860 & rs 8099917 Genotyping Qualitative PCR Test

The purpose of the IL28B Genotyping Test is to determine the genetic variants at rs12979860 and rs80...

🩸Sample: Whole blood
TAT: 2-3 business days

NAFLD - PNPLA3 & TM6SF2 Genotyping Test

To detect genetic variants in PNPLA3 and TM6SF2 genes that are linked to non-alcoholic fatty liver d...

🩸Sample: Whole blood
TAT: 2-3 business days

NR1H4 Gene Cholestasis, infantile, NR1H4 related NGS Genetic Test

To identify mutations in the NR1H4 gene responsible for infantile cholestasis, enabling accurate dia...

🩸Sample: Blood or Extracted DNA or One drop Blood on FTA Card
TAT: 3 to 4 weeks

UGT1A1 Gene Crigler-Najjar syndrome, type 1 NGS Genetic Test

To identify mutations in the UGT1A1 gene that cause Crigler-Najjar Syndrome Type 1, aiding in diagno...

🩸Sample: Blood, Extracted DNA, or FTA Card
TAT: 3 to 4 weeks

UGT1A1 Gene Crigler-Najjar syndrome, type 2 NGS Genetic Test

To identify mutations in the UGT1A1 gene for the diagnosis of Crigler-Najjar Syndrome Type 2, aiding...

🩸Sample: Blood or Extracted DNA or One drop Blood on FTA Card
TAT: 3 to 4 Weeks

ABCC2 Gene Dubin-Johnson syndrome NGS Genetic Test

To diagnose Dubin-Johnson Syndrome by detecting mutations in the ABCC2 gene using NGS technology, ai...

🩸Sample: Blood
TAT: 3 to 4 Weeks

NBAS Gene Infantile liver failure syndrome type 2 NGS Genetic Test

To diagnose infantile liver failure syndrome type 2 by identifying mutations in the NBAS gene using...

🩸Sample: Blood or Extracted DNA or One drop Blood on FTA Card
TAT: 3 to 4 Weeks

Criggler Najjar Syndrome

The purpose of this test is to diagnose Criggler Najjar Syndrome by identifying genetic mutations in...

🩸Sample: Peripheral Blood
TAT: 7-8 days

SP110 Gene Hepatic venoocclusive disease with immunodeficiency NGS Genetic Test

To diagnose mutations in the SP110 gene associated with hepatic venoocclusive disease and immunodefi...

🩸Sample: Blood or Extracted DNA or One drop Blood on FTA Card
TAT: 3 to 4 Weeks

UGT1A1 Gene Gilbert syndrome NGS Genetic Test

To diagnose Gilbert syndrome by identifying mutations in the UGT1A1 gene using next-generation seque...

🩸Sample: Blood, Extracted DNA, or One drop Blood on FTA Card
TAT: 3-4 weeks

SLCO1B1 Gene Hyperbilirubinemia, Rotor type NGS Genetic Test

To diagnose Hyperbilirubinemia, Rotor Type by detecting mutations in the SLCO1B1 gene using NGS tech...

🩸Sample: Blood or Extracted DNA or One drop Blood on FTA Card
TAT: 3 to 4 Weeks

SLCO1B3 Gene Hyperbilirubinemia, Rotor type NGS Genetic Test

To diagnose Rotor type hyperbilirubinemia by identifying pathogenic mutations in the SLCO1B3 gene us...

🩸Sample: Blood or Extracted DNA or One drop Blood on FTA Card
TAT: 3 to 4 Weeks

PRKCSH Gene Polycystic liver disease NGS Genetic Test

To diagnose mutations in the PRKCSH gene associated with polycystic liver disease, enabling early de...

🩸Sample: Blood or Extracted DNA or One drop Blood on FTA Card
TAT: 3 to 4 Weeks
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