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F13A1 Gene Factor XIIIA deficiency NGS Genetic Test

DNA Labs India | ISO 9001:2015 Certified

F13A1 Gene Factor XIIIA deficiency NGS Genetic Test

Short Name: F13A1 Gene Test

Also known as: Factor XIIIA deficiency, F13A1 gene deficiency, Coagulation Factor XIII A deficiency

F13A1 Gene Factor XIIIA deficiency 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.

Next-Generation Sequencing (NGS)🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of the F13A1 Gene Factor XIIIA deficiency NGS Genetic Test is to identify mutations in the F13A1 gene that cause Factor XIIIA deficiency. This test aids in diagnosing the disorder, guiding treatment decisions, assessing family risk, and facilitating genetic counseling for affected individuals and their families.

Test Code
2588
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 special preparation is required. Provide clinical history and undergo genetic counseling as recommended.

Method: Blood draw or saliva sample

Step 2

Laboratory Analysis

A blood sample will be drawn by a trained phlebotomist, or a saliva sample may be collected using a kit.

Step 3

Report Delivery

Apply pressure to the puncture site to stop bleeding. Resume normal activities unless otherwise advised.

Timeline: 3 to 4 Weeks

Patient Instructions

1
Before the Test:Provide clinical history and undergo genetic counseling. No fasting required.
2
During the Test:Sample collection via blood draw or saliva. Procedure is quick and minimally invasive.
3
After the Test:Sample sent to laboratory for analysis. Results available in 3-4 weeks.

About This Test

Who Should Get This Test

The purpose of the F13A1 Gene Factor XIIIA deficiency NGS Genetic Test is to identify mutations in the F13A1 gene that cause Factor XIIIA deficiency. This test aids in diagnosing the disorder, guiding treatment decisions, assessing family risk, and facilitating genetic counseling for affected individuals and their families.

How to Prepare

  • Provide detailed clinical history of the patient
  • Undergo a genetic counseling session to draw a pedigree chart of affected family members
  • Ensure sample is collected in appropriate container and labeled correctly

Doctor's Notes

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

"Genetic testing for F13A1 deficiency is crucial for early diagnosis and management of bleeding disorders, especially in families with a history of unexplained bleeding."

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 sample

Sample Stability

Blood sample: Stable for 24 hours at room temperature
Extracted DNA: Stable for longer periods if stored properly
Sample Rejection Criteria:
  • Sample improperly labeled or contaminated
  • Insufficient sample volume
  • Sample collected in incorrect container

Understanding Your Results

Results from the F13A1 Gene Test indicate the presence or absence of mutations in the F13A1 gene. Interpretation should be done by a qualified geneticist in conjunction with clinical findings.
📊

Positive for pathogenic variant

Confirms diagnosis of Factor XIIIA deficiency; genetic counseling and management recommended

📊

Negative for pathogenic variant

No mutations detected in F13A1 gene; consider other causes if symptoms persist

📊

Variant of uncertain significance

Further testing or family studies may be needed for clarification

⚠️ When to Consult a Doctor:

Consult a doctor if you experience symptoms of bleeding disorders, have a family history of Factor XIIIA deficiency, or receive an abnormal test result for appropriate management and genetic counseling.

Limitations

  • This test detects only mutations in the F13A1 gene; other causes of bleeding disorders may not be identified
  • Variants of uncertain significance may require further evaluation

Risks & Considerations

  • Minimal risk from blood draw, such as slight discomfort or bruising
  • No significant risks associated with genetic testing itself

Interfering Factors

  • Contaminated or degraded DNA sample
  • Recent blood transfusion may affect results

Frequently Asked Questions

What is F13A1 Gene Factor XIIIA deficiency?
It is a rare genetic disorder caused by mutations in the F13A1 gene, leading to deficiency of coagulation factor XIII and impaired blood clotting.
What are the symptoms of this disorder?
Symptoms include easy bruising, excessive bleeding during menstruation or childbirth, bleeding into joints or muscles, and in severe cases, intracranial hemorrhage.
How is the F13A1 Gene Test performed?
The test uses next-generation sequencing (NGS) technology to analyze DNA from a blood or saliva sample for mutations in the F13A1 gene.
What is the cost of the test in India?
The cost is 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 for online bookings 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 does a positive result mean?
A positive result indicates a pathogenic mutation in the F13A1 gene, confirming Factor XIIIA deficiency diagnosis.
Can this disorder be treated?
While there is no cure, management includes factor replacement therapy and precautions to prevent bleeding episodes.
Is genetic counseling required before the test?
Yes, a genetic counseling session is recommended to understand the test, interpret results, and discuss family implications.
Who should get this test?
Individuals with symptoms of bleeding disorders, family history of Factor XIIIA deficiency, or those recommended by a healthcare provider.
Is the test covered by insurance?
Coverage varies; check with your insurance provider. DNA Labs India offers competitive pricing and discounts.
How accurate is the NGS genetic test?
NGS technology provides high accuracy and comprehensive analysis, making it a reliable method for detecting F13A1 gene mutations.
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 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.

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