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CFHR1 Gene Hemolytic uremic syndrome NGS Genetic Test

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CFHR1 Gene Hemolytic uremic syndrome NGS Genetic Test

Short Name: CFHR1 Gene HUS NGS Test

Also known as: CFHR1 Gene Mutation Test, HUS Genetic Test

CFHR1 Gene Hemolytic uremic syndrome 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.

Genetic Test🏠 Home Collection

🩺 Medically Reviewed By

Overview

To diagnose Hemolytic Uremic Syndrome caused by mutations in the CFHR1 gene using NGS technology.

Test Code
5411
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

Provide clinical history and undergo genetic counseling to draw a family pedigree chart.

Method: Venipuncture for blood, or saliva collection

Step 2

Laboratory Analysis

Sample collection via blood draw or saliva.

Step 3

Report Delivery

Sample sent to lab for NGS analysis.

Timeline: 3 to 4 Weeks

Patient Instructions

1
Before the Test:Provide clinical history and undergo genetic counseling to draw a family pedigree chart.
2
During the Test:Sample collection via blood draw or saliva.
3
After the Test:Sample sent to lab for NGS analysis.

About This Test

Who Should Get This Test

To diagnose Hemolytic Uremic Syndrome caused by mutations in the CFHR1 gene using NGS technology.

How to Prepare

  • Fast not required
  • Provide blood or saliva sample
  • Ensure sample is properly labeled

Doctor's Notes

Reviewed by — MBBS, MD (Pathology) · Reg. No. 21521

"Genetic testing for CFHR1 mutations is essential for accurate diagnosis and timely management of Hemolytic Uremic Syndrome."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Collection MethodVenipuncture for blood, or saliva collection
Sample Rejection Criteria:
  • Hemolyzed sample
  • Insufficient sample volume
  • Contaminated sample

Understanding Your Results

Results indicate the presence or absence of mutations in the CFHR1 gene associated with HUS.
📊

Mutation detected

Increased risk of HUS, further clinical evaluation recommended

📊

No mutation detected

Lower risk, but clinical correlation needed

⚠️ When to Consult a Doctor:

If symptoms of HUS are present or if there is a family history of the disorder.

Limitations

  • May not detect all types of mutations
  • Results require genetic counseling
  • Not a standalone diagnostic tool

Risks & Considerations

  • Minor bruising at blood draw site
  • Emotional impact of genetic results

Interfering Factors

  • Sample contamination
  • Degraded DNA
  • Technical errors in sequencing

Compare With Similar Tests

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Frequently Asked Questions

What is the CFHR1 Gene Hemolytic Uremic Syndrome NGS Genetic Test?
It is a genetic test that uses Next Generation Sequencing to detect mutations in the CFHR1 gene, which can cause Hemolytic Uremic Syndrome.
Why is this test recommended?
It is recommended for individuals with symptoms of HUS or a family history of the disorder to confirm a genetic diagnosis.
How is the test performed?
A blood or saliva sample is collected and analyzed using NGS technology to sequence the CFHR1 gene.
What are the symptoms of Hemolytic Uremic Syndrome?
Symptoms include abdominal pain, bloody diarrhea, fatigue, decreased urine output, and unexplained bruises.
How long does it take to receive the results?
Results are typically available within 3 to 4 weeks after sample collection.
Is home sample collection available?
Yes, DNA Labs India offers free home sample collection for this test across India.
What is the cost of the test?
The test costs INR 20000.
Who should consider getting this test?
Individuals with symptoms of HUS, a family history of HUS, or those diagnosed with atypical HUS.
What does a positive test result mean?
A positive result indicates a mutation in the CFHR1 gene, which may increase the risk of developing HUS. Genetic counseling is recommended.
Are there any risks associated with the test?
The test involves minimal risks, such as slight discomfort during blood draw. Emotional impact of results is possible.
How accurate is the NGS genetic test?
NGS is highly accurate for detecting gene mutations, but results should be interpreted in clinical context.
Can this test be used for prenatal diagnosis?
This test is typically for postnatal diagnosis. For prenatal testing, consult a genetic counselor.
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.

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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