Skip to main content
DNA Labs India

PKP2 Gene Arrhythmogenic right ventricular cardiomyopathy type 9 NGS Genetic Test

DNA Labs India | ISO 9001:2015 Certified

PKP2 Gene Arrhythmogenic right ventricular cardiomyopathy type 9 NGS Genetic Test

Short Name: PKP2 Gene ARVC Type 9 NGS Genetic Test

Also known as: PKP2 Gene ARVC Test, ARVC Type 9 Genetic Test, Plakophilin-2 Gene Test

PKP2 Gene Arrhythmogenic right ventricular cardiomyopathy type 9 NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses NGS Technology 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

✍️ Written By

🩺 Medically Reviewed By

Dr SULOCHANA HEMCHANDRA HOLLA

Dr SULOCHANA HEMCHANDRA HOLLA

Consultant Medical Geneticist · Reg: 8532

Last reviewed: September 7, 2026

Overview

The purpose of this test is to detect mutations in the PKP2 gene associated with Arrhythmogenic Right Ventricular Cardiomyopathy Type 9, facilitating early diagnosis, genetic counseling, and personalized management to reduce the risk of sudden cardiac events.

Test Code
2498
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 Technology
Step 1

Sample Collection

No specific preparation is required. Inform the healthcare provider about any medications or medical conditions.

Method: Blood draw or saliva collection

Step 2

Laboratory Analysis

A blood sample will be drawn from a vein in the arm, or a saliva sample will be collected using a kit.

Step 3

Report Delivery

Apply pressure to the puncture site with a cotton ball to prevent bleeding. Resume normal activities.

Timeline: 3 to 4 weeks

Patient Instructions

1
Before the Test:No specific preparation is required. Inform the healthcare provider about any medications or medical conditions.
2
During the Test:A blood sample will be drawn from a vein in the arm, or a saliva sample will be collected using a kit.
3
After the Test:Apply pressure to the puncture site with a cotton ball to prevent bleeding. Resume normal activities.

About This Test

Who Should Get This Test

The purpose of this test is to detect mutations in the PKP2 gene associated with Arrhythmogenic Right Ventricular Cardiomyopathy Type 9, facilitating early diagnosis, genetic counseling, and personalized management to reduce the risk of sudden cardiac events.

How to Prepare

  • Ensure proper patient identification
  • Use sterile collection equipment
  • Label samples correctly
  • Transport samples as per guidelines

Doctor's Notes

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

"Genetic testing for PKP2 is essential for diagnosing ARVC Type 9, enabling early intervention to prevent sudden cardiac death and manage symptoms effectively."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Collection MethodBlood draw or saliva collection

Sample Stability

Room temperature
Sample Rejection Criteria:
  • Hemolyzed or clotted blood sample
  • Insufficient sample volume
  • Improperly labeled or contaminated samples

Understanding Your Results

Results will indicate whether pathogenic variants in the PKP2 gene are detected. Interpretation should be done by a genetic specialist in the context of clinical findings.
📊

Pathogenic variant detected

Confirms genetic predisposition to ARVC Type 9. Clinical evaluation and monitoring are recommended.

📊

Variant of uncertain significance (VUS)

Further testing and family studies may be needed. Clinical correlation is essential.

📊

No pathogenic variant detected

Reduces likelihood of genetic ARVC due to PKP2, but does not exclude other causes. Clinical follow-up may still be indicated.

⚠️ When to Consult a Doctor:

Consult a cardiologist or geneticist if you experience symptoms of ARVC, have a family history of the condition, or receive a positive genetic test result.

Limitations

  • ⚠May not detect all types of mutations (e.g., large deletions)
  • ⚠Results require clinical correlation and genetic counseling
  • ⚠Cannot predict disease severity or onset age

Risks & Considerations

  • ●Minimal risk from blood draw (bruising, infection)
  • ●Psychological impact of genetic results
  • ●Potential for anxiety or stress related to findings

Interfering Factors

  • ●Sample contamination
  • ●Degraded or insufficient DNA
  • ●Technical errors in sequencing

Compare With Similar Tests

TestPKP2 Gene Arrhythmogenic right ventricular cardiomyopathy type 9 NGS Genetic Test
ComparisonPKP2 Gene Arrhythmogenic right ventricular cardiomyopathy type 9 NGS Genetic Test

Frequently Asked Questions

What is the PKP2 Gene ARVC Type 9 NGS Genetic Test?
This test uses next-generation sequencing to analyze the PKP2 gene for mutations associated with Arrhythmogenic Right Ventricular Cardiomyopathy Type 9, a genetic heart disorder.
Why is this test important?
It helps in early diagnosis of ARVC Type 9, enabling timely management to prevent sudden cardiac death and guide treatment decisions.
Who should consider this test?
Individuals with a family history of ARVC, symptoms like palpitations or fainting, or clinical suspicion based on ECG or imaging findings.
How is the test performed?
A blood or saliva sample is collected and analyzed using NGS technology to sequence the PKP2 gene.
What sample is required?
Blood, extracted DNA, or one drop of blood on an FTA card can be used.
Is fasting required?
No, fasting is not required for this test.
How long does it take to get results?
Results are typically available within 3 to 4 weeks after sample collection.
What does a positive result mean?
A positive result indicates a pathogenic variant in the PKP2 gene, suggesting increased risk for ARVC Type 9. Clinical correlation and genetic counseling are recommended.
What does a negative result mean?
A negative result means no pathogenic variants were detected, reducing the likelihood of genetic ARVC due to PKP2, but other causes may still exist.
Is genetic counseling included?
Yes, the test cost includes genetic counseling and interpretation of results by qualified professionals.
What is the cost of the test?
The test costs INR 20,000, which covers the test, genetic counseling, and result interpretation.
Is home sample collection available?
Yes, free home sample collection is available for online bookings across 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.

Related Tests

MMC (Maternal Myopathy with Cardiomyopathy) Mutation Detection Test

₹11,500

LPA Gene Coronary artery disease, susceptibility to NGS Genetic Test

₹20,000

ITIH4 Gene Hypercholesterolemia, susceptibility to NGS Genetic Test

₹20,000

PPP1R17 Gene Hypercholesterolemia, susceptibility to NGS Genetic Test

₹20,000

APOA1 Gene Hypoalphalipoproteinemia NGS Genetic Test

₹20,000

GJC2 Gene Lymphedema, hereditary, type IC NGS Genetic Test

₹20,000
For Hospitals & Clinics

Reference Laboratory Services

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.

Book Your Test

Enter your details and we'll connect you within 15 minutes.

🧬

Quick Connect

Enter your mobile number and we’ll connect you with the team.

+91

✅ Connecting you now...

🔒 Your number is used to respond to this request.