Nx Gen Sequencing: Albinism Test
Short Name: Albinism Genetic Test
Also known as: Albinism Genetic Sequencing Test, Albinism DNA Test
Nx Gen Sequencing: Albinism Test test available at DNA Labs India for ₹28,665. Uses NGS, Sanger Sequencing on Whole Blood samples. Results in 45 working days from sample receipt. Free home collection in 300+ cities across India.
🩺 Medically Reviewed By
Dr SHAILAJA RAGHUNATH MURDESHWAR
Consultant Physician · Reg: 8052
Last reviewed: September 7, 2026
Overview
The purpose of the Nx Gen Sequencing: Albinism Test is to confirm a diagnosis of albinism, identify the specific genetic mutations involved, and guide clinical management. It helps differentiate between types of albinism, informs prognosis, and supports genetic counseling for affected individuals and their families.
- Test Code
- 1326
- Price
- ₹28,665
- Sample Type
- Whole Blood
- Result Time
- 45 working days from sample receipt
- Fasting Required
- No
- Method
- NGS, Sanger Sequencing
Sample Collection
Duly filled Whole Exome Sequencing Consent Form (Form 37) is mandatory. No fasting required.
Method: Venipuncture
Laboratory Analysis
Blood sample will be collected via venipuncture from a vein in the arm.
Report Delivery
Apply pressure to the collection site to prevent bleeding. Monitor for any signs of bruising or discomfort.
Timeline: 45 working days from sample receipt
Patient Instructions
About This Test
Who Should Get This Test
The purpose of the Nx Gen Sequencing: Albinism Test is to confirm a diagnosis of albinism, identify the specific genetic mutations involved, and guide clinical management. It helps differentiate between types of albinism, informs prognosis, and supports genetic counseling for affected individuals and their families.
How to Prepare
- Submit 10 mL (5 mL min.) whole blood from 2 Lavender Top (EDTA) tubes.
- Ship refrigerated. DO NOT FREEZE.
- Ensure tubes are properly labeled and sealed.
Doctor's Notes
Reviewed by Dr SHAILAJA RAGHUNATH MURDESHWAR — MBBS, MD (General Medicine) · Reg. No. 8052
"Genetic testing for albinism aids in precise diagnosis and family planning. Early identification through Nx Gen Sequencing can guide management and genetic counseling."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Insufficient sample volume
- Hemolyzed or clotted samples
- Missing consent form
- Improperly labeled tubes
Understanding Your Results
Pathogenic mutation detected
Confirms diagnosis of albinism; further clinical evaluation recommended.
No pathogenic mutations detected
Albinism less likely; consider other diagnoses or repeat testing if symptoms persist.
Variant of uncertain significance (VUS)
Genetic variant found but clinical significance unknown; genetic counseling advised.
Consult a doctor if you or your child has symptoms of albinism, such as very light skin, vision problems, or sensitivity to light, or for genetic counseling after test results.
Limitations
- ⚠May not detect all possible genetic variants or mutations
- ⚠Results require clinical correlation
- ⚠Not suitable for prenatal diagnosis without additional confirmation
Risks & Considerations
- ●Minor bruising or pain at the blood draw site
- ●Rare risk of infection or fainting
Interfering Factors
- ●Sample contamination
- ●Insufficient sample volume
- ●Improper sample storage or handling
Compare With Similar Tests
| Test | Nx Gen Sequencing: Albinism Test | Clinical Examination | Single Gene Testing | Whole Exome Sequencing | Skin Biopsy |
|---|---|---|---|---|---|
| Comparison | Nx Gen Sequencing: Albinism Test |
Frequently Asked Questions
What is the Nx Gen Sequencing: Albinism Test?
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What sample is required for the test?
Is fasting required before the test?
How long does it take to get the results?
What are the symptoms of albinism that indicate this test?
Can this test identify the type of albinism?
Is home sample collection available?
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₹20,000Reference 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.
✓ DPDP Act Compliant: Under the Digital Personal Data Protection Act 2023, you can request deletion of your records at any time by contacting support.
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