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GGCX Gene Vitamin K-dependent clotting factors combined deficiency type 1 NGS Genetic Test

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GGCX Gene Vitamin K-dependent clotting factors combined deficiency type 1 NGS Genetic Test

Short Name: GGCX Gene NGS Genetic Test

Also known as: Vitamin K-dependent clotting factors combined deficiency type 1, GGCX deficiency, Hereditary combined deficiency of vitamin K-dependent clotting factors

GGCX Gene Vitamin K-dependent clotting factors combined deficiency type 1 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 from sample receipt. Free home collection in 300+ cities across India.

Genetic TestAll Ages🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of this test is to diagnose GGCX gene mutations responsible for vitamin K-dependent clotting factors combined deficiency type 1, enabling early intervention, personalized treatment, and genetic counseling for affected individuals and their families.

Test Code
2693
Price
₹20,000
Sample Type
Blood or Extracted DNA or One drop Blood on FTA Card
Result Time
3 to 4 weeks from sample receipt
Fasting Required
No
Method
Next-Generation Sequencing (NGS)
Step 1

Sample Collection

Provide detailed clinical history and undergo genetic counseling to draw a pedigree chart of affected family members.

Method: Venipuncture or finger prick

Step 2

Laboratory Analysis

A blood sample is collected via venipuncture or finger prick, or a drop of blood is placed on an FTA card.

Step 3

Report Delivery

The sample is labeled, stored at appropriate temperature, and sent to the laboratory for DNA extraction and NGS analysis.

Timeline: 3 to 4 weeks from sample receipt

Patient Instructions

1
Before the Test:Genetic counseling and clinical history review are recommended before sample collection.
2
During the Test:The test involves DNA extraction from the blood sample followed by NGS sequencing of the GGCX gene.
3
After the Test:Results are analyzed by geneticists, and a clinical report is generated. Genetic counseling is advised to discuss findings.

About This Test

Who Should Get This Test

The purpose of this test is to diagnose GGCX gene mutations responsible for vitamin K-dependent clotting factors combined deficiency type 1, enabling early intervention, personalized treatment, and genetic counseling for affected individuals and their families.

How to Prepare

  • Ensure patient provides complete clinical history
  • Schedule genetic counseling session prior to testing
  • Use sterile collection techniques
  • Label samples accurately

Doctor's Notes

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

"Genetic testing for GGCX mutations is essential for diagnosing rare clotting disorders, enabling personalized management and family counseling."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Sample VolumeAs required for DNA extraction
ContainerEDTA tube or FTA card
Collection MethodVenipuncture or finger prick

Sample Stability

Blood samples stable for 24 hours at room temperature; store at 2-8°C for longer delays
FTA cards stable at room temperature for extended periods
Sample Rejection Criteria:
  • Hemolyzed or clotted samples
  • Insufficient sample volume
  • Incorrect labeling or missing documentation

Understanding Your Results

Results from the GGCX Gene NGS Genetic Test indicate the presence or absence of mutations in the GGCX gene. Positive results confirm the diagnosis of vitamin K-dependent clotting factors combined deficiency type 1, while negative results may require further testing if clinical suspicion remains.
Pathogenic variants detected: Confirms diagnosis; refer for hematological management and genetic counseling.
No pathogenic variants detected: Does not rule out other causes; consider additional tests.
Variants of uncertain significance: May require family studies or functional assays for clarification.
⚠️ When to Consult a Doctor:

Consult a hematologist or genetic specialist if you experience symptoms of bleeding disorders, have a family history of clotting deficiencies, or receive abnormal test results.

Limitations

  • May not detect all genetic variants or mutations
  • Results require interpretation by a genetic specialist
  • Does not replace clinical evaluation for bleeding disorders

Risks & Considerations

  • Minor bruising or discomfort at the blood draw site
  • Rare risk of infection
  • Emotional impact of genetic results

Interfering Factors

  • Sample degradation or contamination
  • Recent blood transfusions
  • Use of anticoagulant medications
  • Improper sample storage

Compare With Similar Tests

TestGGCX Gene Vitamin K-dependent clotting factors combined deficiency type 1 NGS Genetic TestProthrombin Time (PT) TestPartial Thromboplastin Time (PTT) TestFactor Activity Assays
ComparisonGGCX Gene Vitamin K-dependent clotting factors combined deficiency type 1 NGS Genetic Test

Frequently Asked Questions

What is the GGCX Gene NGS Genetic Test?
It is a genetic test that uses Next-Generation Sequencing to analyze the GGCX gene for mutations causing vitamin K-dependent clotting factors deficiency type 1.
Who should consider this test?
Individuals with symptoms like easy bruising, nosebleeds, or heavy menstrual bleeding, or those with a family history of clotting disorders.
What are the common symptoms of GGCX deficiency?
Symptoms include bruising easily, nosebleeds, bleeding gums, excessive bleeding after injury, heavy periods, and blood in urine or stool.
How is the test performed?
A blood sample is collected, DNA is extracted, and the GGCX gene is sequenced using NGS technology.
What is the cost of the test?
The test costs INR 20,000 at DNA Labs India, with home sample collection available.
Is home sample collection available?
Yes, DNA Labs India offers free home sample collection across many cities in India.
How long does it take to get results?
Results are typically available within 3 to 4 weeks after sample collection.
What do the test results mean?
Results indicate the presence or absence of GGCX gene mutations. Positive results confirm the diagnosis, while negative results may require further evaluation.
Is genetic counseling necessary?
Yes, genetic counseling is recommended before and after testing to understand implications, family risks, and management options.
Can this test detect all mutations?
While NGS is comprehensive, it may not detect all possible genetic variants or mutations in the GGCX gene.
Is the test covered by insurance?
Coverage varies by insurance plan; it is advisable to check with your provider. DNA Labs India offers transparent pricing.
How accurate is the test?
NGS technology is highly accurate for detecting genetic mutations, but results should be interpreted by a qualified genetic specialist.
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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