FAM20A Gene Amelogenesis imperfecta type 1G NGS Genetic Test
Short Name: FAM20A AI Type 1G NGS Test
Also known as: FAM20A Gene Test for Amelogenesis Imperfecta Type 1G
FAM20A Gene Amelogenesis imperfecta 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 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 identify mutations in the FAM20A gene to diagnose amelogenesis imperfecta type 1G, enabling personalized treatment plans and genetic counseling for affected individuals and families.
- Test Code
- 4831
- 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
No special preparation required. Provide clinical history and family pedigree if available.
Method: Venipuncture or finger prick
Laboratory Analysis
Standard blood draw or saliva collection procedure.
Report Delivery
Apply pressure to the puncture site to stop bleeding. Store sample as instructed.
Timeline: 3 to 4 weeks
Patient Instructions
About This Test
Who Should Get This Test
The purpose of this test is to identify mutations in the FAM20A gene to diagnose amelogenesis imperfecta type 1G, enabling personalized treatment plans and genetic counseling for affected individuals and families.
How to Prepare
- Use sterile equipment
- Label sample correctly
- Transport at ambient temperature
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"This test is essential for accurate diagnosis and personalized management of amelogenesis imperfecta type 1G, guiding treatment and genetic counseling."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed or insufficient sample volume
- Improper labeling
- Contaminated sample
Understanding Your Results
Positive for pathogenic variants
Confirms diagnosis of AI type 1G. Genetic counseling and dental management recommended.
Negative for pathogenic variants
No mutations detected in FAM20A gene. Consider other genetic or environmental causes.
Variant of uncertain significance
Further testing and family studies may be needed for clarification.
Consult a dentist or genetic specialist if you experience dental symptoms like enamel defects, sensitivity, or have a family history of amelogenesis imperfecta.
Limitations
- ⚠May not detect all genetic variants
- ⚠Requires genetic counseling for interpretation
- ⚠Results should be correlated with clinical findings
Risks & Considerations
- ●Minimal risk from blood draw, such as bruising or infection
- ●Psychological impact of genetic results
Interfering Factors
- ●Sample contamination
- ●Degraded DNA
- ●Improper sample storage
Compare With Similar Tests
| Test | FAM20A Gene Amelogenesis imperfecta type 1G NGS Genetic Test | AMELX Gene Test | Dental Enamel Disorder Panel |
|---|---|---|---|
| Comparison | FAM20A Gene Amelogenesis imperfecta type 1G NGS Genetic Test |
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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