AR Gene Androgen insensitivity NGS Genetic Test
Short Name: AR Gene Androgen Insensitivity Test
Also known as: Androgen Receptor Gene Test, AIS Genetic Test, AR Gene Sequencing
AR Gene Androgen insensitivity 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 Androgen Insensitivity Syndrome and related disorders by identifying mutations in the AR gene using NGS technology.
- Test Code
- 5365
- 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
Clinical history of the patient and a genetic counseling session to draw a pedigree chart of family members affected with AR gene-related conditions.
Method: Venipuncture or FTA Card
Laboratory Analysis
Standard blood draw or FTA card collection procedure performed by a trained phlebotomist.
Report Delivery
Sample is processed for DNA extraction and analyzed using NGS technology in the laboratory.
Timeline: 3 to 4 weeks
Patient Instructions
About This Test
Who Should Get This Test
To diagnose Androgen Insensitivity Syndrome and related disorders by identifying mutations in the AR gene using NGS technology.
How to Prepare
- Provide detailed clinical history
- Attend genetic counseling session
- Ensure proper sample collection and labeling
- Follow fasting instructions if applicable
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"This test is crucial for diagnosing androgen insensitivity syndrome, guiding treatment and genetic counseling for affected individuals and families."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed samples
- Insufficient sample volume
- Contaminated samples
Understanding Your Results
Positive
Pathogenic variant detected, indicating Androgen Insensitivity Syndrome or related disorder.
Negative
No pathogenic variants detected, suggesting no genetic basis for AIS.
Variant of Uncertain Significance
Genetic variant found but clinical significance is unknown; further testing may be needed.
If symptoms of AIS are present, such as ambiguous genitalia or infertility, or if there is a family history of the condition.
Limitations
- ⚠May not detect all types of mutations
- ⚠Requires genetic counseling for accurate interpretation
- ⚠Results may have variants of uncertain significance
Risks & Considerations
- ●Minimal risk from blood draw, such as bruising or infection
- ●Genetic privacy concerns
- ●Emotional impact of results
Interfering Factors
- ●Sample contamination
- ●Degraded DNA
- ●Incorrect sample handling
Compare With Similar Tests
| Test | AR Gene Androgen insensitivity NGS Genetic Test | Karyotype Test | Hormone Panel | FISH for AR gene | Whole Exome Sequencing |
|---|---|---|---|---|---|
| Comparison | AR Gene Androgen insensitivity NGS Genetic Test | Detects chromosomal abnormalities but may not identify specific gene mutations. | Measures hormone levels but does not provide genetic diagnosis. | Targets specific mutations but less comprehensive than NGS. | Broader genetic analysis but more costly and time-consuming. |
Frequently Asked Questions
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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.
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.
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