SLC35C1 Gene Glycosylation disorder type 2C NGS Genetic Test
Short Name: SLC35C1 Gene Glycosylation Disorder 2C Test
SLC35C1 Gene Glycosylation disorder type 2C 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 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 test is to detect mutations in the SLC35C1 gene to confirm a diagnosis of Glycosylation Disorder Type 2C, guide treatment decisions, and provide genetic counseling for affected individuals and their families.
- Test Code
- 2051
- 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
- Next Generation Sequencing (NGS)
Sample Collection
A genetic counseling session is recommended to understand the test implications and draw a pedigree chart of family history. Provide clinical history of the patient.
Method: Phlebotomy
Laboratory Analysis
Sample is collected via blood draw or saliva swab by a trained phlebotomist. For FTA card, a drop of blood is applied.
Report Delivery
Sample is processed and sent to the laboratory for analysis. Keep the site clean and dry if blood was drawn.
Timeline: 3 to 4 Weeks
Patient Instructions
About This Test
Who Should Get This Test
The purpose of this test is to detect mutations in the SLC35C1 gene to confirm a diagnosis of Glycosylation Disorder Type 2C, guide treatment decisions, and provide genetic counseling for affected individuals and their families.
How to Prepare
- Ensure patient is relaxed and hydrated before blood draw
- Use sterile equipment for collection
- Label samples correctly with patient details
- For FTA card, follow specific instructions for blood application
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"Early diagnosis through genetic testing is crucial for the management and treatment planning of SLC35C1 Gene Glycosylation Disorder Type 2C."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed or clotted blood samples
- Contaminated or improperly labeled samples
- Insufficient sample volume
Understanding Your Results
No pathogenic variants detected
No mutations associated with the disorder were found. Clinical correlation is advised.
Pathogenic variant detected
Confirms diagnosis of SLC35C1 Gene Glycosylation Disorder Type 2C. Genetic counseling recommended.
Variant of uncertain significance
Further testing or family studies may be needed for clarification.
Consult a doctor or genetic counselor if the test results are positive, if symptoms persist, or for family planning advice after diagnosis.
Limitations
- ⚠May not detect all genetic variants, such as large deletions or duplications
- ⚠Requires confirmation with additional methods for certain variants
- ⚠Results should be interpreted in conjunction with clinical findings
Risks & Considerations
- ●Minor bruising or discomfort at the blood draw site
- ●Low risk of infection from needle stick
Interfering Factors
- ●Poor sample quality
- ●Contamination during collection
- ●Insufficient DNA quantity
Frequently Asked Questions
What is SLC35C1 Gene Glycosylation Disorder Type 2C?
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Reference 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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