APOA1 Gene Amyloidosis, familial visceral NGS Genetic Test
Short Name: APOA1 Amyloidosis Genetic Test
Also known as: Apolipoprotein A1 Amyloidosis, Familial Visceral Amyloidosis, APOA1-Related Amyloidosis
APOA1 Gene Amyloidosis, familial visceral NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses NGS (Next-Generation Sequencing) 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 APOA1 gene that cause familial visceral amyloidosis, aiding in diagnosis, prognosis, genetic counseling, and informing treatment strategies.
- Test Code
- 1887
- 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 (Next-Generation Sequencing)
Sample Collection
Clinical history review and genetic counselling session recommended to draw a pedigree chart of family members affected with amyloidosis.
Method: Venipuncture
Laboratory Analysis
Standard blood draw procedure following aseptic techniques.
Report Delivery
Sample is processed and analyzed in the laboratory using NGS technology.
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 APOA1 gene that cause familial visceral amyloidosis, aiding in diagnosis, prognosis, genetic counseling, and informing treatment strategies.
How to Prepare
- Use sterile collection equipment
- Label the sample correctly with patient details
- Transport at ambient room temperature as specified
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"This test is crucial for early diagnosis and management of familial amyloidosis, aiding in family planning, treatment decisions, and genetic counseling."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed or clotted samples
- Insufficient sample volume
- Incorrect or missing labeling
- Contaminated samples
Understanding Your Results
Pathogenic variant detected
Confirms diagnosis of APOA1 gene amyloidosis. Genetic counseling and management by a specialist recommended.
No pathogenic variant detected
Does not rule out other forms of amyloidosis or genetic causes. Clinical correlation and additional testing may be advised.
Variant of uncertain significance (VUS)
Further testing, family studies, or functional analysis may be needed for classification.
If you experience symptoms such as organ enlargement, heart problems, kidney issues, or neuropathy, especially with a family history of amyloidosis, consult a geneticist or specialist for evaluation.
Limitations
- ⚠This test may not detect all mutations in the APOA1 gene or other genes causing amyloidosis
- ⚠Results require clinical correlation and interpretation by a geneticist
- ⚠Cannot predict disease severity, age of onset, or progression rate
Risks & Considerations
- ●Minimal risk from blood draw, such as bruising or infection
- ●Potential psychological impact from genetic results, addressed through counseling
Interfering Factors
- ●Poor sample quality or contamination
- ●Inadequate DNA extraction
- ●Sample mishandling during transport
Compare With Similar Tests
| Test | APOA1 Gene Amyloidosis, familial visceral NGS Genetic Test | TTR Gene Amyloidosis Test | SAA Gene Test |
|---|---|---|---|
| Comparison | APOA1 Gene Amyloidosis, familial visceral NGS Genetic Test |
Frequently Asked Questions
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