SLCO1B1 Gene Hyperbilirubinemia, Rotor type NGS Genetic Test
Short Name: SLCO1B1 Rotor Type NGS Test
Also known as: Rotor syndrome, SLCO1B1-related hyperbilirubinemia
SLCO1B1 Gene Hyperbilirubinemia, Rotor type NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses NGS Technology on Blood or Extracted DNA or One drop Blood on FTA Card samples. Results in 3 to 4 Weeks. Free home collection in 300+ cities across India.
🩺 Medically Reviewed By
Dr SULOCHANA HEMCHANDRA HOLLA
Consultant Medical Geneticist · Reg: 8532
Last reviewed: September 7, 2026
Overview
To diagnose Hyperbilirubinemia, Rotor Type by detecting mutations in the SLCO1B1 gene using NGS technology, aiding in clinical management and genetic counseling.
- Test Code
- 5424
- Price
- ₹20,000
- Sample Type
- Blood or Extracted DNA or One drop Blood on FTA Card
- Result Time
- 3 to 4 Weeks
- Fasting Required
- No
- Method
- NGS Technology
Sample Collection
Genetic counseling session recommended to discuss test implications and draw a family pedigree chart.
Method: Venipuncture or FTA card collection
Laboratory Analysis
Blood sample collected via venipuncture or one drop on FTA card by a trained phlebotomist.
Report Delivery
Apply pressure to the puncture site; sample sent to lab for analysis.
Timeline: 3 to 4 Weeks
Patient Instructions
About This Test
Who Should Get This Test
To diagnose Hyperbilirubinemia, Rotor Type by detecting mutations in the SLCO1B1 gene using NGS technology, aiding in clinical management and genetic counseling.
How to Prepare
- Ensure proper identification and consent
- Use sterile equipment for blood draw
- Label samples correctly with patient details
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"This test is crucial for diagnosing Rotor type hyperbilirubinemia, a rare genetic disorder affecting bilirubin metabolism, and guides appropriate clinical management."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Insufficient sample volume
- Hemolyzed or contaminated samples
- Incorrect labeling or missing patient information
Understanding Your Results
Mutation Detected
Confirms diagnosis of Rotor type hyperbilirubinemia; genetic counseling and management recommended.
No Mutation Detected
Reduces likelihood of Rotor type hyperbilirubinemia; consider other causes of symptoms.
Consult a doctor if you experience symptoms like jaundice, dark urine, or have a family history of liver disorders, and after receiving test results for further guidance.
Limitations
- ⚠May not detect all genetic variants or mutations
- ⚠Results require interpretation by a genetic specialist
- ⚠Does not rule out other causes of hyperbilirubinemia
Risks & Considerations
- ●Minor bruising or discomfort at blood draw site
- ●Rare risk of infection
- ●Emotional impact of genetic results
Interfering Factors
- ●Sample contamination
- ●Degraded DNA quality
- ●Incorrect sample collection or handling
Frequently Asked Questions
What is SLCO1B1 Gene Hyperbilirubinemia, Rotor Type NGS Genetic Test?
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Who should get this test?
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₹27,000Reference Laboratory Services
We serve as a reference laboratory for hospitals and clinics across India. Send samples from your facility with same-day pickup, priority processing, and results delivered through our online portal. Competitive institutional pricing available.
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✓ Stored in India: All patient records are stored on servers located in India. No data is transferred outside the country.
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