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DNA Labs India

Whole Genome Test

DNA Labs India | ISO 9001:2015 Certified

Whole Genome Test

Short Name: WGS Test

Also known as: Whole Genome Sequencing, WGS, Genetic Mapping Test

Whole Genome Test test available at DNA Labs India for ₹130,000. Uses SNP Genotyping using Microarray on Whole Blood samples. Results in Reports are typically available within 8 weeks after sample collection.. Free home collection in 300+ cities across India.

Genetic Mapping🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of the Whole Genome Test is to identify genetic variations that may indicate predispositions to diseases, aiding in accurate diagnosis, personalized treatment strategies, and informed family planning. It helps in understanding the genetic basis of symptoms and conditions, providing a foundation for preventive healthcare measures.

Test Code
659
Price
₹130,000
Sample Type
Whole Blood
Result Time
Reports are typically available within 8 weeks after sample collection.
Fasting Required
No
Method
SNP Genotyping using Microarray
Step 1

Sample Collection

Ensure the Genome Mapping Consent Form (Form 26) is duly filled. No specific preparation needed, but consult with a genetic counselor if unsure.

Method: Venipuncture

Step 2

Laboratory Analysis

A blood sample will be drawn via venipuncture by a trained phlebotomist. The process is quick and minimally invasive.

Step 3

Report Delivery

Apply pressure to the puncture site to prevent bleeding. Resume normal activities unless advised otherwise.

Timeline: Reports are typically available within 8 weeks after sample collection.

Patient Instructions

1
Before the Test:Fill the consent form and discuss any concerns with a genetic counselor.
2
During the Test:Blood sample collection is performed in a sterile environment.
3
After the Test:Results will be available in 8 weeks. Genetic counseling is recommended to interpret results.

About This Test

Who Should Get This Test

The purpose of the Whole Genome Test is to identify genetic variations that may indicate predispositions to diseases, aiding in accurate diagnosis, personalized treatment strategies, and informed family planning. It helps in understanding the genetic basis of symptoms and conditions, providing a foundation for preventive healthcare measures.

How to Prepare

  • Fast for 8-10 hours if specified, though not mandatory for this test.
  • Bring the filled consent form to the collection center.
  • Stay hydrated before sample collection.

Doctor's Notes

Reviewed by — MBBS, MD (Medical Genetics) · Reg. No. 8532

"Early detection through whole genome testing can significantly improve management of genetic conditions and inform family planning decisions."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeWhole Blood
Sample Volume3 mL (2 mL min.)
Container1 Lavender top (EDTA) tube
Collection MethodVenipuncture

Sample Stability

Room Temperature24 hours
Refrigerated72 hours
FrozenNot applicable
Sample Rejection Criteria:
  • Insufficient sample volume
  • Missing or incomplete consent form
  • Labeled incorrectly

Understanding Your Results

Results from the Whole Genome Test provide a detailed report on genetic variations. Interpretation should be done by a qualified geneticist or healthcare provider to understand implications for health and treatment.
📊

No pathogenic variants detected

Indicates no known genetic predisposition for tested conditions.

📊

Pathogenic variant identified

May indicate a genetic disorder or carrier status; consult a genetic counselor for further guidance.

⚠️ When to Consult a Doctor:

Consult a doctor or genetic counselor if you have a family history of genetic disorders, exhibit symptoms mentioned, or receive abnormal results from this test.

Limitations

  • May not detect all genetic disorders
  • Requires duly filled Genome Mapping Consent Form (Form 26)
  • Results may require further confirmatory testing

Risks & Considerations

  • Minimal risk associated with blood draw, such as bruising or infection
  • Psychological impact from potential findings

Interfering Factors

  • Sample contamination
  • Improper sample storage
  • Incomplete consent form

Compare With Similar Tests

TestWhole Genome TestWhole Exome SequencingChromosomal MicroarraySingle Gene Test
ComparisonWhole Genome Test

Frequently Asked Questions

What is the cost of the Whole Genome Test?
The Whole Genome Test costs INR 130,000 at DNA Labs India, with free home sample collection available in many cities across India.
How long does it take to get the results?
Results are typically available within 8 weeks after sample collection.
What sample is required for this test?
A blood sample of 3 mL (minimum 2 mL) in an EDTA tube is required.
Is fasting required for the Whole Genome Test?
No, fasting is not required, but ensure the consent form is duly filled.
What are the symptoms that might indicate the need for this test?
Symptoms include developmental delays, intellectual disabilities, abnormal facial features, recurrent infections, abnormal growth, seizures, chronic pain, and behavioral problems.
Who should consider taking the Whole Genome Test?
Individuals with a family history of genetic disorders, those exhibiting symptoms of genetic conditions, or for family planning purposes.
How is the test performed?
The test involves SNP Genotyping using Microarray technology to analyze DNA variations across the entire genome.
Are there any risks associated with the test?
Risks are minimal, similar to a standard blood draw, such as bruising or infection at the puncture site. Psychological impact from potential findings is also possible.
Can this test diagnose all genetic disorders?
While comprehensive, it may not detect all genetic disorders. Confirmatory testing might be needed for certain conditions.
Is genetic counseling provided with the test?
Yes, DNA Labs India offers genetic counseling to help interpret test results and guide next steps.
How do I prepare for the test?
Fill out the Genome Mapping Consent Form (Form 26) and bring it to the collection center. No other special preparation is needed.
What happens if the test results are abnormal?
If pathogenic variants are detected, consult a genetic counselor or healthcare provider for further evaluation, management options, and potential family screening.
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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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.

LIMS Integration

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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