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DNA Labs India

HBA2 Gene Thalassemia, alpha NGS Genetic Test

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HBA2 Gene Thalassemia, alpha NGS Genetic Test

Short Name: HBA2 Gene Thalassemia NGS Test

Also known as: HBA2 Gene Test, Alpha Thalassemia Genetic Test, Thalassemia Alpha NGS Test

HBA2 Gene Thalassemia, alpha 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.

NGS Genetic TestAll Ages🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of the HBA2 Gene Thalassemia NGS Genetic Test is to identify pathogenic mutations in the HBA2 gene associated with alpha thalassemia. This aids in accurate diagnosis, assessment of carrier status, prenatal screening, and personalized treatment planning. It helps healthcare providers and patients understand genetic risks and make informed decisions regarding health management and family planning.

Test Code
5629
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)
Step 1

Sample Collection

Provide clinical history and undergo genetic counseling to draw a pedigree chart. No fasting is required.

Step 2

Laboratory Analysis

A blood sample will be collected via venipuncture or using an FTA card for one drop of blood.

Step 3

Report Delivery

Apply pressure to the puncture site to prevent bruising. Resume normal activities immediately.

Timeline: 3 to 4 Weeks

Patient Instructions

1
Before the Test:Understand the test purpose through genetic counseling. Provide detailed clinical and family history.
2
During the Test:A blood sample is drawn; the process is quick and minimally invasive.
3
After the Test:Wait for report delivery in 3-4 weeks. Discuss results with a healthcare provider.

About This Test

Who Should Get This Test

The purpose of the HBA2 Gene Thalassemia NGS Genetic Test is to identify pathogenic mutations in the HBA2 gene associated with alpha thalassemia. This aids in accurate diagnosis, assessment of carrier status, prenatal screening, and personalized treatment planning. It helps healthcare providers and patients understand genetic risks and make informed decisions regarding health management and family planning.

How to Prepare

  • Ensure proper identification and labeling of the sample
  • Use sterile collection tubes or FTA cards as specified
  • Transport samples at ambient room temperature to the lab

Doctor's Notes

Reviewed by — MBBS, MD (Pathology) · Reg. No. 21521

"Genetic testing for HBA2 gene mutations is essential for accurate diagnosis, carrier screening, and informed family planning in alpha thalassemia cases."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card

Sample Stability

Blood samples are stable for up to 7 days at room temperature
Extracted DNA can be stored at -20°C for long-term use
Sample Rejection Criteria:
  • Hemolyzed or clotted blood samples
  • Insufficient sample volume
  • Improperly labeled or contaminated samples

Understanding Your Results

Results indicate the presence or absence of mutations in the HBA2 gene. A positive result confirms genetic variants associated with alpha thalassemia, while a negative result suggests no detectable pathogenic mutations.
📊

No pathogenic variants detected

Normal; no mutations in HBA2 gene linked to alpha thalassemia

📊

Pathogenic variant detected

Carrier or affected status for alpha thalassemia; clinical correlation and genetic counseling recommended

📊

Variant of uncertain significance

Further testing or family studies may be needed for clarification

⚠️ When to Consult a Doctor:

Consult a doctor or genetic counselor if you have a family history of thalassemia, experience symptoms like persistent anemia, or receive a positive test result for guidance on management and family planning.

Limitations

  • May not detect all rare or novel mutations in the HBA2 gene
  • Results require interpretation by a genetic counselor or healthcare provider
  • Does not assess mutations in other thalassemia-related genes like HBA1

Risks & Considerations

  • Minimal risk from blood draw, such as slight pain, bruising, or infection at the puncture site

Interfering Factors

  • Poor sample quality or insufficient DNA
  • Contamination during sample collection or processing
  • Recent blood transfusions may affect DNA analysis

Frequently Asked Questions

What is the HBA2 Gene Thalassemia NGS Genetic Test?
It is a genetic test that uses next-generation sequencing to detect mutations in the HBA2 gene, which is associated with alpha thalassemia, a blood disorder affecting hemoglobin production.
Who should consider this test?
Individuals with a family history of thalassemia, symptoms of anemia, or those seeking carrier screening, especially from high-prevalence regions.
What is the cost of the test?
The test costs INR 20000 at DNA Labs India, with home sample collection available across India.
How is the test performed?
A blood sample is collected and analyzed using NGS technology to identify mutations in the HBA2 gene.
What are the symptoms of alpha thalassemia?
Symptoms include anemia, fatigue, pale skin, shortness of breath, jaundice, bone deformities, and enlarged spleen, varying by mutation severity.
How long does it take to get results?
Reports are typically delivered within 3 to 4 weeks after sample collection.
Is fasting required for this test?
No, fasting is not required for the HBA2 Gene Thalassemia NGS Genetic Test.
Can this test diagnose all types of thalassemia?
No, it specifically targets alpha thalassemia related to HBA2 gene mutations. Other tests may be needed for beta thalassemia or HBA1 mutations.
What do the results mean?
Results indicate the presence or absence of HBA2 gene mutations. A positive result suggests carrier or affected status, while negative means no detectable pathogenic variants.
Is genetic counseling recommended?
Yes, genetic counseling is advised before and after testing to understand implications, especially for family planning.
Does DNA Labs India provide raw data files?
Yes, DNA Labs India shares raw data, FASTQ, and VCF files along with the clinical report for transparency.
Is home sample collection available?
Yes, free home sample collection is offered for online bookings across numerous cities in India.
Worried about the process? Our certified phlebotomists collect thousands of samples every month across India. The process takes under 5 minutes and is virtually painless. Questions? Message us on WhatsApp — we're here 7 days a week.

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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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