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SPINK1 Gene Pancreatitis NGS Genetic Test

DNA Labs India | ISO 9001:2015 Certified

SPINK1 Gene Pancreatitis NGS Genetic Test

Short Name: SPINK1 Gene Test

Also known as: SPINK1 Mutation Test, Hereditary Pancreatitis Genetic Test, SPINK1 Gene Analysis

SPINK1 Gene Pancreatitis 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 SPINK1 Gene Pancreatitis NGS Genetic Test is to detect mutations in the SPINK1 gene to confirm a diagnosis of hereditary pancreatitis, guide treatment decisions, assess risk for family members, and facilitate genetic counseling.

Test Code
5475
ICD Code
K85.9
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, but provide clinical history and family pedigree during genetic counseling.

Method: Venipuncture or FTA Card Spot

Step 2

Laboratory Analysis

A blood sample will be drawn from a vein in the arm, or a blood spot will be collected on an FTA card.

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:Undergo genetic counseling to understand the test implications and provide family history.
2
During the Test:Sample collection takes about 10-15 minutes. The test itself is laboratory-based and non-invasive.
3
After the Test:Wait for 3-4 weeks for results. Discuss findings with a genetic counselor or physician.

About This Test

Who Should Get This Test

The purpose of the SPINK1 Gene Pancreatitis NGS Genetic Test is to detect mutations in the SPINK1 gene to confirm a diagnosis of hereditary pancreatitis, guide treatment decisions, assess risk for family members, and facilitate genetic counseling.

How to Prepare

  • Ensure the patient is relaxed and hydrated for blood draw
  • Use sterile equipment for sample collection
  • Label the sample correctly with patient details
  • For FTA card, allow blood to dry completely before packaging

Doctor's Notes

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

"This test is essential for families with a history of pancreatitis to identify genetic risks early and guide preventive care."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Sample Volume3-5 mL
ContainerEDTA Tube or FTA Card
Collection MethodVenipuncture or FTA Card Spot

Sample Stability

Blood sample stable for 48 hours at room temperature
Extracted DNA stable for up to 1 year at -20°C
FTA card samples stable for several years at room temperature
Sample Rejection Criteria:
  • Hemolyzed or clotted blood sample
  • Insufficient sample volume
  • Incorrect labeling or missing patient information
  • Sample contaminated or improperly stored

Understanding Your Results

Results indicate whether pathogenic mutations in the SPINK1 gene are detected. A positive result confirms genetic predisposition to pancreatitis, while a negative result suggests no known mutations, but does not exclude other causes.
📊

Pathogenic variant detected

Confirms diagnosis of SPINK1-related hereditary pancreatitis. Recommend clinical management and family screening.

📊

No pathogenic variant detected

No mutations found in the SPINK1 gene. Consider other genetic or environmental factors for pancreatitis symptoms.

📊

Variant of uncertain significance (VUS)

A genetic change was found, but its clinical significance is unclear. Further testing and monitoring may be needed.

⚠️ When to Consult a Doctor:

Consult a doctor if you experience symptoms of pancreatitis, have a family history of the condition, or receive a positive test result for appropriate management and genetic counseling.

Limitations

  • May not detect all possible mutations in the SPINK1 gene
  • Results require interpretation by a genetic specialist
  • Does not rule out other genetic or environmental causes of pancreatitis
  • Limited to known pathogenic variants in current databases

Risks & Considerations

  • Minimal risk from blood draw, such as slight pain or bruising
  • Psychological impact of genetic results
  • Potential for uncertain results requiring further investigation

Interfering Factors

  • Contaminated or degraded DNA sample
  • Recent blood transfusion affecting DNA composition
  • Improper sample storage or handling
  • Use of certain medications that may alter DNA integrity

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ComparisonSPINK1 Gene Pancreatitis NGS Genetic Test

Frequently Asked Questions

What is the SPINK1 Gene Pancreatitis NGS Genetic Test?
It is a genetic test that uses Next-Generation Sequencing to detect mutations in the SPINK1 gene, which can cause hereditary pancreatitis.
Who should consider this test?
Individuals with a family history of pancreatitis, recurrent pancreatitis symptoms, or those seeking genetic counseling for hereditary conditions.
What is the cost of the test?
The test costs INR 20000, which includes sample collection, analysis, and report delivery.
How is the sample collected?
A blood sample is drawn from the arm, or a blood spot is collected on an FTA card. Home collection is available across India.
Is fasting required before the test?
No, fasting is not required for this genetic test.
How long does it take to get results?
Results are typically available within 3 to 4 weeks after sample collection.
What do the results mean?
A positive result indicates a pathogenic mutation in the SPINK1 gene, confirming hereditary pancreatitis risk. A negative result means no known mutations were found.
Is the test painful?
The blood draw may cause slight discomfort, but the test itself is non-invasive and performed in a laboratory.
Can this test be done at home?
Yes, DNA Labs India offers free home sample collection for online bookings across many cities in India.
What should I do after receiving the results?
Consult a genetic counselor or physician to interpret the results and discuss management options, including family screening.
Is the test covered by insurance?
Coverage varies by insurance provider and scheme. It is not typically covered under government schemes like PMJAY, but check with your insurer.
Why choose DNA Labs India for this test?
DNA Labs India provides transparent reporting with raw data, FASTQ, and VCF files, along with clinical reports, and offers nationwide home collection.
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.

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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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