WDR36 Gene Glaucoma, Open Angle Type 1G NGS Genetic Test
Short Name: WDR36 Glaucoma NGS Test
Also known as: WDR36 Gene Sequencing, Glaucoma Open Angle Type 1G Genetic Test, POAG1G NGS Test, WDR36 Mutation Analysis
WDR36 Gene Glaucoma, Open Angle Type 1G NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses Next Generation Sequencing (NGS) on Blood or Extracted DNA or One drop Blood on FTA Card samples. Results in Samples are processed after receipt and reports are delivered within 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
The purpose of this NGS genetic test is to detect sequence variants in the WDR36 gene that are associated with primary open-angle glaucoma type 1G. Testing may help confirm a genetic contribution in patients with clinically diagnosed open-angle glaucoma, identify presymptomatic at-risk family members, and guide early monitoring and treatment decisions.
- Test Code
- 3834
- Price
- ₹20,000
- Sample Type
- Blood or Extracted DNA or One drop Blood on FTA Card
- Result Time
- Samples are processed after receipt and reports are delivered within 3 to 4 weeks.
- Fasting Required
- No
- Method
- Next Generation Sequencing (NGS)
Sample Collection
No fasting is required. Clinical history and a genetic counselling session are recommended before giving the sample. Continue all medications unless instructed otherwise by your doctor.
Method: Venipuncture / Finger-prick FTA card / Pre-extracted DNA
Laboratory Analysis
Blood is drawn by a trained phlebotomist using a sterile needle. If using an FTA card, a simple finger-prick blood spot is applied to the labelled card.
Report Delivery
The sample is sent to the DNA Labs India laboratory. Reports are shared via portal, email and WhatsApp in 3 to 4 weeks. A genetic counsellor is available if you need help understanding your result.
Timeline: Samples are processed after receipt and reports are delivered within 3 to 4 weeks.
Patient Instructions
About This Test
Who Should Get This Test
The purpose of this NGS genetic test is to detect sequence variants in the WDR36 gene that are associated with primary open-angle glaucoma type 1G. Testing may help confirm a genetic contribution in patients with clinically diagnosed open-angle glaucoma, identify presymptomatic at-risk family members, and guide early monitoring and treatment decisions.
How to Prepare
- No special preparation or fasting is required.
- Use an EDTA tube for venous blood; minimum 2 mL is recommended.
- For FTA card, apply one drop of blood to each marked circle and air-dry.
- If providing extracted DNA, use a DNase-free tube and send in cold storage.
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"Genetic testing for WDR36 variants is most useful when combined with a detailed eye examination and genetic counselling. A positive result should prompt regular intraocular pressure checks and optic nerve evaluation in the patient and at-risk relatives."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Clotted blood sample in EDTA tube.
- Insufficient blood volume or DNA quantity.
- Incorrectly labelled sample or missing patient details.
- Wet, stained, or contaminated FTA card.
- Sample container broken during transport.
Understanding Your Results
Positive / Pathogenic variant
A disease-associated variant was detected. The patient has an increased susceptibility to open-angle glaucoma type 1G. Closer ophthalmological monitoring is recommended.
Positive / Likely pathogenic variant
A variant likely to be disease-causing was detected. Clinical segregation and family correlation are required.
Negative
No pathogenic/likely pathogenic variant was found in WDR36. A hereditary cause in this gene is less likely; other genes or causes may be considered.
Variant of uncertain significance (VUS)
A genetic variant of uncertain clinical significance was found. It cannot be classified as pathogenic or benign based on current evidence. Further family studies may help.
Inconclusive
DNA analysis did not achieve adequate quality or coverage; repeat testing or a new sample may be necessary.
If you have a positive or uncertain result, consult an ophthalmologist and a clinical geneticist. Any symptoms such as gradual vision loss, tunnel vision, halos, or eye pain require prompt medical evaluation.
Limitations
- ⚠WDR36 variants have variable penetrance and are not fully causative; the result improves risk assessment but does not diagnose glaucoma by itself.
- ⚠A negative WDR36 test does not exclude mutations in other glaucoma genes or non-genetic causes.
- ⚠Variants of uncertain significance may lack definitive clinical actionability.
- ⚠Results should always be interpreted by a clinical geneticist in the context of family history and ophthalmological evaluation.
Risks & Considerations
- ●Minor bruising or pain at the blood collection site.
- ●Possible psychological stress from genetic findings.
- ●Implications for blood relatives that may require discussion.
- ●No significant other physical risks from sample collection.
Interfering Factors
- ●Variants in non-coding, deep intronic or regulatory regions may not be covered by this targeted test.
- ●Large genomic deletions, duplications or structural variants may not be detected by standard NGS.
- ●Low-level mosaic variants below the sensitivity of the assay may be missed.
- ●Poor DNA quality or sample degradation due to improper transport may affect results.
Compare With Similar Tests
| Test | WDR36 Gene Glaucoma, Open Angle Type 1G NGS Genetic Test | |||||
|---|---|---|---|---|---|---|
| Comparison | WDR36 Gene Glaucoma, Open Angle Type 1G NGS Genetic Test |
Frequently Asked Questions
What is WDR36 gene glaucoma?
What is the cost of this NGS genetic test at DNA Labs India?
What sample is required?
Is fasting needed before the test?
Who should consider this test?
Will I receive raw data?
How long does the test report take?
Does this test detect all glaucoma gene mutations?
What do negative test results mean?
Is home sample collection available?
Is genetic counselling recommended?
Is the test covered by insurance or government schemes?
Related Tests
Leber's Hereditary Optic Neuropathy (LHON) Mitochondrial Mutation Detection Test
₹25,000Nx Gen Sequencing: Glaucoma Test
₹28,665Nx Gen Sequencing: Corneal Dystrophy Test
₹28,665Nx Gen Sequencing: Leber Congenital Amaurosis Test
₹28,665Nx Gen Sequencing: Optic Atrophy Test
₹28,665GPR143 Gene Albinism, Ocular Type I, Nettleship-Falls Type NGS Genetic Test
₹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.
Your Data Privacy
Your medical data is protected under Indian law.
✓ 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.
Book Your Test
Enter your details and we'll connect you within 15 minutes.
