Skip to main content
DNA Labs India

SLC29A3 Gene Histiocytosis-lymphadenopathy plus syndrome NGS Genetic Test

DNA Labs India | ISO 9001:2015 Certified

SLC29A3 Gene Histiocytosis-lymphadenopathy plus syndrome NGS Genetic Test

Short Name: SLC29A3 HLAS NGS Test

Also known as: Histiocytosis-lymphadenopathy plus syndrome, HLAS

SLC29A3 Gene Histiocytosis-lymphadenopathy plus syndrome 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 3-4 weeks. Free home collection in 300+ cities across India.

Next-Generation Sequencing (NGS)🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of this test is to identify pathogenic mutations in the SLC29A3 gene to confirm a diagnosis of Histiocytosis-lymphadenopathy plus syndrome (HLAS), guide treatment decisions, and facilitate genetic counseling for affected individuals and their families.

Test Code
4964
Price
₹20,000
Sample Type
Blood or Extracted DNA or One drop Blood on FTA Card
Result Time
3-4 weeks
Fasting Required
No
Method
Next-Generation Sequencing (NGS)
Step 1

Sample Collection

Clinical history of the patient and a genetic counseling session to draw a pedigree chart of family members affected with HLAS are recommended before testing.

Method: Venipuncture or FTA card

Step 2

Laboratory Analysis

Standard blood draw procedure using venipuncture or collection of a blood drop on an FTA card. No special preparation is required.

Step 3

Report Delivery

Apply pressure to the puncture site to prevent bleeding. Store samples as per instructions for stability.

Timeline: 3-4 weeks

Patient Instructions

1
Before the Test:Genetic counseling and clinical history review are essential before testing.
2
During the Test:Sample collection via blood draw or FTA card; no pain beyond standard venipuncture.
3
After the Test:Results are available online; follow-up with a healthcare provider for interpretation and next steps.

About This Test

Who Should Get This Test

The purpose of this test is to identify pathogenic mutations in the SLC29A3 gene to confirm a diagnosis of Histiocytosis-lymphadenopathy plus syndrome (HLAS), guide treatment decisions, and facilitate genetic counseling for affected individuals and their families.

How to Prepare

  • No fasting required
  • Bring valid ID and prescription
  • Ensure sample is properly labeled
  • For FTA card, follow specific instructions for blood application

Doctor's Notes

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

"Genetic testing for HLAS is crucial for early diagnosis and management. Consult with a genetic counselor for family planning and treatment options."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Sample VolumeVaries
ContainerEDTA tube or FTA card
Collection MethodVenipuncture or FTA card

Sample Stability

Blood: Store at 2-8°C for up to 48 hours
FTA card: Store at room temperature for extended periods
Extracted DNA: Store at -20°C for long-term
Sample Rejection Criteria:
  • Hemolyzed or clotted sample
  • Insufficient sample volume
  • Improperly labeled or contaminated samples

Understanding Your Results

Results indicate the presence or absence of mutations in the SLC29A3 gene. Interpretation should be done by a qualified geneticist or healthcare provider.
📊

No pathogenic variants detected

Negative for SLC29A3 mutations; HLAS unlikely but clinical correlation is advised.

📊

Pathogenic or likely pathogenic variant detected

Confirms diagnosis of HLAS; genetic counseling and treatment planning recommended.

📊

Variant of uncertain significance (VUS)

Further testing or family studies may be needed; clinical management based on symptoms.

⚠️ When to Consult a Doctor:

Consult a geneticist, immunologist, or dermatologist if symptoms persist, worsen, or if there is a family history of HLAS. Genetic counseling is advised for all positive results.

Limitations

  • May not detect all types of mutations (e.g., large deletions/duplications)
  • Results require interpretation by a genetic counselor or specialist
  • Does not rule out other genetic or non-genetic causes of symptoms

Risks & Considerations

  • Minimal risk from blood draw (e.g., bruising, infection)
  • Psychological impact of genetic results
  • Potential for uncertain results requiring further testing

Interfering Factors

  • Sample contamination
  • Degraded DNA
  • Hemolyzed blood sample

Compare With Similar Tests

TestSLC29A3 Gene Histiocytosis-lymphadenopathy plus syndrome NGS Genetic TestWhole Exome SequencingTargeted Gene Panel for ImmunodeficiencySanger Sequencing
ComparisonSLC29A3 Gene Histiocytosis-lymphadenopathy plus syndrome NGS Genetic Test

Frequently Asked Questions

What is the SLC29A3 Gene Histiocytosis-lymphadenopathy plus syndrome NGS Genetic Test?
It is a genetic test that uses next-generation sequencing to detect mutations in the SLC29A3 gene, which causes HLAS, a rare immune disorder.
Who should get this test?
Individuals with symptoms like swollen lymph nodes, skin rash, fever, or enlarged liver/spleen, or those with a family history of HLAS.
What is the cost of the test in India?
The test costs INR 20,000, with free home sample collection available across India.
How is the sample collected?
Sample is collected via blood draw or using a blood drop on an FTA card. Home collection is offered.
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 3-4 weeks after sample collection.
What do the results mean?
Results indicate if pathogenic mutations are present in the SLC29A3 gene. A positive result confirms HLAS diagnosis.
Is genetic counseling recommended?
Yes, genetic counseling is strongly recommended before and after testing to understand implications and family planning.
What files are provided with the report?
DNA Labs India provides raw data, FASTQ, and VCF files along with the clinical test report for transparency.
Can this test be done for children?
Yes, the test is suitable for all ages, but pediatric cases should be guided by a healthcare provider.
Is the test covered by insurance?
Coverage varies; check with your insurance provider. Government schemes like PMJAY may not cover it.
What are the risks of the test?
Risks are minimal, mainly related to blood draw (e.g., bruising). Psychological impact of results is possible.
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.

Related Tests

For Hospitals & Clinics

Reference Laboratory Services

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.

LIMS Integration

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.

Book Your Test

Enter your details and we'll connect you within 15 minutes.

🧬

Quick Connect

Enter your mobile number and we’ll connect you with the team.

+91

✅ Connecting you now...

🔒 Your number is used to respond to this request.