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SLX4 Gene Fanconi anemia type P NGS Genetic Test

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SLX4 Gene Fanconi anemia type P NGS Genetic Test

Short Name: SLX4 FA Type P NGS Test

Also known as: Fanconi Anemia Type P Genetic Test, SLX4 Mutation Analysis, FA Type P NGS Test

SLX4 Gene Fanconi anemia type P 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.

NGS Genetic TestUnisexAll Ages🏠 Home Collection

🩺 Medically Reviewed By

Overview

To diagnose Fanconi Anemia Type P by identifying mutations in the SLX4 gene using NGS technology, aiding in clinical management and genetic counseling.

Test Code
1991
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

No special preparation required. Genetic counseling recommended before test.

Method: Venipuncture or Capillary Blood on FTA Card

Step 2

Laboratory Analysis

Blood sample will be drawn by a trained phlebotomist.

Step 3

Report Delivery

Apply pressure to the puncture site. Resume normal activities.

Timeline: 3 to 4 weeks from sample receipt.

Patient Instructions

1
Before the Test:Genetic counseling to understand implications. Provide clinical history and family details.
2
During the Test:Blood draw followed by DNA extraction and NGS analysis in the laboratory.
3
After the Test:Results reviewed by a geneticist. Follow-up counseling recommended based on findings.

About This Test

Who Should Get This Test

To diagnose Fanconi Anemia Type P by identifying mutations in the SLX4 gene using NGS technology, aiding in clinical management and genetic counseling.

How to Prepare

  • Ensure proper patient identification
  • Use sterile collection equipment
  • Label sample correctly with patient details

Doctor's Notes

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

"Genetic testing for Fanconi Anemia is essential for early intervention and family planning. The SLX4 gene test helps identify carriers and affected individuals."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Collection MethodVenipuncture or Capillary Blood on FTA Card

Sample Stability

Room Temperature
Refrigerated
Sample Rejection Criteria:
  • Hemolyzed sample
  • Insufficient sample volume
  • Incorrect container or labeling

Understanding Your Results

Results should be interpreted by a qualified geneticist in the context of clinical findings and family history.
Positive result: Pathogenic mutation detected, confirms diagnosis of Fanconi Anemia Type P.
Negative result: No mutation detected, but does not rule out other genetic causes.
Variant of uncertain significance: Requires further investigation and genetic counseling.
⚠️ When to Consult a Doctor:

Consult a geneticist or hematologist if you have symptoms of Fanconi Anemia, a positive test result, or a family history of the disorder.

Limitations

  • May not detect all types of mutations
  • False negatives possible
  • Cannot determine disease severity

Risks & Considerations

  • Minimal risk from blood draw (e.g., bruising)
  • Potential psychological impact of results
  • Insurance or privacy considerations

Interfering Factors

  • Sample contamination
  • Poor DNA quality
  • Hemolyzed blood sample

Compare With Similar Tests

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Frequently Asked Questions

What is Fanconi Anemia Type P?
Fanconi Anemia Type P is a rare genetic disorder caused by mutations in the SLX4 gene, leading to bone marrow failure and increased cancer risk.
What is the SLX4 gene?
The SLX4 gene encodes a protein involved in DNA repair. Mutations in this gene cause Fanconi Anemia Type P.
What are the symptoms of Fanconi Anemia Type P?
Symptoms include anemia, low platelet count, neutropenia, increased infections, cancer risk, skeletal abnormalities, developmental delays, and short stature.
How is Fanconi Anemia Type P diagnosed?
Diagnosis typically involves genetic testing, such as the SLX4 Gene NGS Test, along with blood tests and bone marrow biopsy.
What is the SLX4 Gene Fanconi Anemia Type P NGS Genetic Test?
It is a genetic test using next-generation sequencing to detect mutations in the SLX4 gene for accurate diagnosis.
How much does the test cost?
The test costs INR 20,000 at DNA Labs India, including genetic counseling.
What sample type is required?
Blood, extracted DNA, or one drop of blood on an FTA card.
How long does it take to get results?
Results are available in 3 to 4 weeks.
Is home sample collection available?
Yes, free home collection is available across India for online bookings.
What does a positive test result mean?
A positive result indicates a pathogenic mutation in the SLX4 gene, confirming Fanconi Anemia Type P diagnosis.
Is genetic counseling included?
Yes, genetic counseling is included in the test cost.
How can I book the test?
You can book online through DNA Labs India website or contact their customer service.
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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