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PRKAR1A Gene Myxoma, intracardiac NGS Genetic Test

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PRKAR1A Gene Myxoma, intracardiac NGS Genetic Test

Short Name: PRKAR1A Myxoma NGS Test

Also known as: PRKAR1A Mutation Test, Cardiac Myxoma Genetic Test, Intracardiac Myxoma NGS Test

PRKAR1A Gene Myxoma, intracardiac 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 PRKAR1A Gene Myxoma NGS Genetic Test is to identify mutations in the PRKAR1A gene that are associated with the development of cardiac myxomas. This test aids in confirming a genetic diagnosis, assessing risk for family members, and guiding clinical management to prevent complications such as stroke or heart failure.

Test Code
2908
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

No specific preparation required. Ensure genetic counseling is completed and clinical history is provided.

Method: Venipuncture or Fingerstick

Step 2

Laboratory Analysis

A blood sample will be collected via venipuncture or a fingerstick for FTA card. The process is quick and minimally invasive.

Step 3

Report Delivery

Apply pressure to the collection site to prevent bleeding. Resume normal activities immediately.

Timeline: 3 to 4 Weeks

Patient Instructions

1
Before the Test:Complete genetic counseling and provide clinical history. No fasting required unless specified.
2
During the Test:Blood sample collection takes about 10-15 minutes. The test involves NGS analysis of DNA.
3
After the Test:Results are available in 3-4 weeks. Follow up with a healthcare provider for interpretation.

About This Test

Who Should Get This Test

The purpose of the PRKAR1A Gene Myxoma NGS Genetic Test is to identify mutations in the PRKAR1A gene that are associated with the development of cardiac myxomas. This test aids in confirming a genetic diagnosis, assessing risk for family members, and guiding clinical management to prevent complications such as stroke or heart failure.

How to Prepare

  • Provide informed consent for genetic testing.
  • Share detailed family medical history.
  • Avoid eating or drinking for 30 minutes before blood draw if specified.

Doctor's Notes

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

"This NGS genetic test is essential for identifying PRKAR1A gene mutations linked to cardiac myxomas, aiding in early diagnosis and family screening."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Sample VolumeAs required
ContainerEDTA Tube or FTA Card
Collection MethodVenipuncture or Fingerstick

Sample Stability

Room TemperatureUp to 48 hours for blood samples
RefrigeratedUp to 7 days for extracted DNA
Sample Rejection Criteria:
  • Insufficient sample volume
  • Hemolyzed or clotted blood samples
  • Incorrect labeling or missing documentation

Understanding Your Results

Results from the PRKAR1A Gene Myxoma NGS Genetic Test indicate the presence or absence of mutations in the PRKAR1A gene. A positive result confirms a genetic predisposition to cardiac myxomas, while a negative result suggests no detected mutations, though clinical correlation is advised.
📊

Positive for PRKAR1A mutation

Confirms genetic cause of cardiac myxoma; recommend family screening and cardiac monitoring.

📊

Negative for PRKAR1A mutation

No pathogenic variant detected; consider other genetic or environmental factors.

📊

Variant of uncertain significance

Further testing and clinical evaluation recommended.

⚠️ When to Consult a Doctor:

Consult a doctor if you experience symptoms like chest pain, shortness of breath, or heart palpitations, or if you have a family history of cardiac myxomas. After receiving test results, seek genetic counseling for personalized management.

Limitations

  • This test does not detect all genetic variants associated with cardiac myxomas.
  • Results may require confirmation with additional testing.
  • Genetic variants of uncertain significance may be identified.

Risks & Considerations

  • Minimal risk from blood draw, such as bruising or infection.
  • Psychological impact of genetic results, including anxiety.
  • Potential for incidental findings unrelated to myxoma.

Interfering Factors

  • Contaminated or degraded DNA samples
  • Recent blood transfusions
  • Technical errors in sequencing

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Frequently Asked Questions

What is the PRKAR1A Gene Myxoma NGS Genetic Test?
This test uses next-generation sequencing to detect mutations in the PRKAR1A gene, which are linked to cardiac myxomas, noncancerous heart tumors.
Who should consider this test?
Individuals with a family history of cardiac myxomas, symptoms like chest pain or palpitations, or diagnosed with intracardiac myxoma.
How is the test performed?
A blood or DNA sample is collected and analyzed using NGS technology to identify PRKAR1A gene mutations.
What is the cost of the test in India?
The test costs INR 20000, with free home sample collection available across India.
How long does it take to get results?
Results are typically available within 3 to 4 weeks after sample collection.
Is fasting required before the test?
No, fasting is not required for this genetic test.
What do the results mean?
A positive result indicates a PRKAR1A mutation, confirming genetic predisposition to cardiac myxoma. A negative result means no mutation was detected.
Can this test be done at home?
Yes, DNA Labs India offers free home sample collection for online bookings in many cities across India.
Is the test accurate?
Yes, NGS technology provides high accuracy for detecting genetic mutations, but results should be interpreted by a healthcare professional.
What are the risks of the test?
Risks are minimal, such as bruising from blood draw, but there may be psychological impacts from genetic results.
How do I prepare for the test?
No special preparation is needed. Provide your clinical history and complete genetic counseling if required.
What should I do after receiving results?
Consult a doctor or genetic counselor to understand the results and discuss management options, including 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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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.

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