Introduction
With DNA testing becoming popular, the need to understand your genealogy and heritage is increasing. If you want to test your DNA, you'll probably wonder how much it will cost. Curious about what price tag a DNA test comes with? Knowing the cost of a DNA test in India can help you make an informed decision, especially if the budget is a concern. Please keep reading to know more about the costs of these tests and how much money you're likely to spend on them.
Cost in Top Cities
| Cities | Min | Avg | Max |
|---|---|---|---|
| Delhi | $9 | $562 | $1116 |
| Ahmedabad | $7 | $470 | $932 |
| Bengaluru | $9 | $552 | $1096 |
| Mumbai | $9 | $583 | $1157 |
| Pune | $8 | $531 | $1055 |
| Chennai | $8 | $506 | $1004 |
| Hyderabad | $8 | $490 | $973 |
| Kolkata | $7 | $449 | $891 |
Top Hospitals
More Information
How much does a DNA test cost in India?
A DNA test can help you understand your genetic makeup. It will tell you about your ethnicity, family relationships, and how you might be susceptible to certain diseases.
The DNA test price in India ranges from 25,00 INR to 20,000 INR, depending on some factors. In comparison, there isn't a specific cost that you can expect your DNA test to come with.
Other Details
Factors affecting DNA testing cost in India:
Multiple factors determine the cost of getting your DNA tested in India. Here are some that you should be aware of
The type of DNA test you want: Different types of DNA tests have different prices.
The company you go with: Prices vary from company to company. Some companies might be more expensive than others, depending on their brand name.
How quickly you want your results: You can get your DNA results in as little as a week or as long as three months. The quicker you want your results, the more you'll need to pay. DNA laboratories tend to charge more for expedited services.
Types of DNA tests
Diagnostic testing-
Presymptomatic and predictive testing: This testing is done to identify gene mutations related to disorders that appear after birth or often later in life.
Carrier testing: This testing can help you detect genes associated with diseases and can also identify if your partner is also a carrier of the same conditions.
Pharmacogenetics: This testing is used to examine the patient's genetic buildup to identify what medicine and dosage are beneficial and suitable for the patient.
Prenatal testing: Used to determine the fetus's genes or chromosomes before birth.
Newborn screening: This testing is done to identify some genetic and metabolic abnormalities that cause specific disorders.
Preimplantation testing: This test is generally used if individuals try to conceive a child through in-vitro fertilization.
Diagnostic testing: This testing is done to identify whether a person has a particular genetic or chromosomal condition.
Non-diagnostic testing-
Forensic testing: This testing uses DNA sequences for legal purposes.
Paternity testing: This testing is used to identify similar inheritance between related individuals.
Genealogical testing: Used to determine ancient or ethnic heritage for genetic genealogy.
Disclaimer : The above rates are for reference purpose only and may vary based on different requirements. To know actual rates, please contact us.
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