RABGGTA Gene Autism Spectrum Disorder NGS Genetic Test
Short Name: RABGGTA Gene ASD NGS Test
Also known as: RABGGTA Gene Sequencing, Autism Spectrum Disorder NGS Panel, RABGGTA ASD Genetic Test
RABGGTA Gene Autism Spectrum Disorder 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 Results are typically delivered within 3 to 4 weeks after the sample reaches the laboratory. The report includes variant details, classification, and downloadable raw data files (FASTQ, VCF).. 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 the RABGGTA gene NGS genetic test is to identify pathogenic mutations in the RABGGTA gene that may be associated with Autism Spectrum Disorder. This test aids clinicians in establishing a molecular diagnosis, guiding appropriate management, enabling early intervention, and facilitating informed genetic counseling for the patient and family members.
- Test Code
- 3897
- CPT Code
- 81479
- ICD Code
- F84.0
- Price
- ₹20,000
- Sample Type
- Blood or Extracted DNA or One drop Blood on FTA Card
- Result Time
- Results are typically delivered within 3 to 4 weeks after the sample reaches the laboratory. The report includes variant details, classification, and downloadable raw data files (FASTQ, VCF).
- Fasting Required
- No
- Method
- Next-Generation Sequencing (NGS)
Sample Collection
No special preparation, including fasting, is required. Please carry any previous genetic test reports, clinical history, and physician referral if available. A genetic counseling session will be conducted to draw a pedigree chart.
Method: Peripheral blood draw or FTA card spot
Laboratory Analysis
For blood sample, a standard peripheral blood draw is performed. If using FTA card, a small drop of blood is applied onto the card. The process is painless and takes about 5 minutes.
Report Delivery
You may resume normal activities immediately. The collected sample will be transported to our accredited laboratory. Reports will be shared via email/WhatsApp within the turnaround time.
Timeline: Results are typically delivered within 3 to 4 weeks after the sample reaches the laboratory. The report includes variant details, classification, and downloadable raw data files (FASTQ, VCF).
Patient Instructions
About This Test
Who Should Get This Test
The purpose of the RABGGTA gene NGS genetic test is to identify pathogenic mutations in the RABGGTA gene that may be associated with Autism Spectrum Disorder. This test aids clinicians in establishing a molecular diagnosis, guiding appropriate management, enabling early intervention, and facilitating informed genetic counseling for the patient and family members.
How to Prepare
- Use EDTA vacutainer for blood collection
- For FTA card, ensure the card is properly labeled and dried
- Samples should be transported at room temperature
- Do not freeze whole blood; extracted DNA should be stored at -20°C
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"A multidisciplinary approach with pediatric neurology and clinical genetics is recommended to interpret this test, assess developmental milestones, and guide early intervention and family counseling."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Clotted or hemolyzed blood samples
- Improperly labeled samples
- Insufficient DNA quantity or quality
- Samples received in non-EDTA tubes (heparin or citrate)
Understanding Your Results
Pathogenic variant detected
Variant is disease-causing and likely contributes to ASD. Genetic counseling recommended.
Likely pathogenic variant detected
Variant is likely disease-causing but additional evidence may be needed. Clinical correlation advised.
Variant of uncertain significance (VUS)
Variant cannot be classified as benign or pathogenic. Further family studies may help.
No pathogenic variant detected
No disease-associated variant found in the RABGGTA gene. Does not rule out ASD.
If the test identifies a pathogenic or likely pathogenic variant, please consult a clinical geneticist and a neurologist/developmental pediatrician for further management, surveillance, and family counseling.
Limitations
- ⚠This test does not detect all genetic causes of ASD
- ⚠Variants of uncertain significance may require further testing or family segregation analysis
- ⚠Non-genetic and environmental factors are not evaluated
- ⚠The test is limited to the RABGGTA gene and does not screen other ASD-related genes
Risks & Considerations
- ●Minimal risk of bruising or bleeding at the puncture site
- ●Slight discomfort during blood draw
- ●Rare risk of infection (very low)
- ●Fainting or dizziness in rare cases
Interfering Factors
- ●Poor DNA quality or quantity from sample
- ●Contamination during sample collection or processing
- ●Incomplete clinical information restricting interpretation
- ●Presence of mosaic variants below sequencing depth threshold
Compare With Similar Tests
| Test | RABGGTA Gene Autism Spectrum Disorder NGS Genetic Test | Single Gene Sequencing | ASD NGS Panel | Whole Exome Sequencing |
|---|---|---|---|---|
| Comparison | RABGGTA Gene Autism Spectrum Disorder NGS Genetic Test |
Frequently Asked Questions
What is the RABGGTA gene?
How is Autism Spectrum Disorder diagnosed?
What is the cost of the RABGGTA gene NGS genetic test at DNA Labs India?
What sample is required for this test?
Do I need to fast before the test?
How long will it take to get the test reports?
What is Next-Generation Sequencing (NGS)?
Will I get raw data files like FASTQ and VCF?
Does DNA Labs India provide home sample collection?
Is genetic counseling required before the test?
What are the common symptoms of Autism Spectrum Disorder?
Can this test definitively diagnose Autism Spectrum Disorder?
Related Tests
Angelman Syndrome Test
₹10,000Duchenne / Becker Muscular Dystrophy (DMD / BMD) Gene Mutation Test
₹14,000Episodic Ataxia Type 1 Hotspot Test
₹11,500Episodic Ataxia Comprehensive Profile Hotspot Test
₹16,000Megalencephalic Leukoencephalopathy with Subcortical Cysts Van Der Knaap and Nalband MLC Gene Hotspot Mutation Test
₹7,500Analyzer 18 SMA 18 Test Panel
₹1,755Reference 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.
