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LRRC6 Gene Primary ciliary dyskinesia type 19 NGS Genetic Test

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LRRC6 Gene Primary ciliary dyskinesia type 19 NGS Genetic Test

Short Name: LRRC6 Gene PCD Type 19 NGS Test

Also known as: Primary Ciliary Dyskinesia Type 19 NGS Test, LRRC6 Gene Mutation Test

LRRC6 Gene Primary ciliary dyskinesia type 19 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)All Ages🏠 Home Collection

🩺 Medically Reviewed By

Overview

To diagnose Primary Ciliary Dyskinesia Type 19 by detecting pathogenic mutations in the LRRC6 gene using next-generation sequencing technology.

Test Code
4776
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

Provide clinical history and undergo genetic counseling if recommended.

Method: Venipuncture or FTA card collection

Step 2

Laboratory Analysis

Blood sample collected via venipuncture or FTA card as per standard procedure.

Step 3

Report Delivery

Sample is labeled and sent to the laboratory for analysis.

Timeline: 3 to 4 weeks

Patient Instructions

1
Before the Test:Genetic counseling is recommended to understand implications and family history.
2
During the Test:Blood sample is analyzed using next-generation sequencing to sequence the LRRC6 gene.
3
After the Test:Report is generated and delivered; follow-up consultation advised.

About This Test

Who Should Get This Test

To diagnose Primary Ciliary Dyskinesia Type 19 by detecting pathogenic mutations in the LRRC6 gene using next-generation sequencing technology.

How to Prepare

  • Ensure proper sample labeling
  • Avoid hemolysis in blood sample
  • Follow instructions for FTA card if used

Doctor's Notes

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

"This test is crucial for diagnosing PCD Type 19, especially in families with a history of respiratory issues or situs inversus."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Sample VolumeAs per requirement
ContainerEDTA tube or FTA card
Collection MethodVenipuncture or FTA card collection

Sample Stability

Blood: 2-8°C for 48 hours
FTA card: Stable at room temperature
Sample Rejection Criteria:
  • Hemolyzed sample
  • Insufficient volume
  • Improper labeling
  • Contaminated sample

Understanding Your Results

Results indicate the presence or absence of pathogenic mutations in the LRRC6 gene associated with PCD Type 19.
📊

Pathogenic variant detected

Confirms diagnosis of PCD Type 19; genetic counseling recommended.

📊

No pathogenic variant detected

PCD Type 19 unlikely based on this gene, but clinical correlation and further testing may be needed.

⚠️ When to Consult a Doctor:

If symptoms persist, family history of PCD, or results indicate mutations, consult a geneticist or pulmonologist.

Limitations

  • May not detect all possible mutations
  • Requires genetic counseling for interpretation
  • Results should be correlated with clinical findings

Risks & Considerations

  • Minimal risk from blood draw (bruising, infection)
  • Genetic implications for family members

Interfering Factors

  • Sample contamination
  • Degraded DNA
  • Hemolyzed blood sample

Compare With Similar Tests

TestLRRC6 Gene Primary ciliary dyskinesia type 19 NGS Genetic TestPCD Panel NGS TestSanger Sequencing for LRRC6
ComparisonLRRC6 Gene Primary ciliary dyskinesia type 19 NGS Genetic Test

Frequently Asked Questions

What is the LRRC6 Gene PCD Type 19 NGS Genetic Test?
It is a diagnostic test that uses next-generation sequencing to detect mutations in the LRRC6 gene, which cause Primary Ciliary Dyskinesia Type 19.
How much does the test cost in India?
The cost is approximately INR 20000 at DNA Labs India.
What sample type is required for the test?
Blood, extracted DNA, or one drop of blood on an FTA card.
How long does it take to get results?
Results are typically available within 3 to 4 weeks.
Is home sample collection available?
Yes, free home sample collection is offered for online bookings across India.
What are the symptoms of PCD Type 19?
Symptoms include chronic respiratory infections, sinusitis, frequent ear infections, hearing loss, and situs inversus totalis.
How is PCD Type 19 inherited?
It is inherited in an autosomal recessive manner, requiring two copies of the mutated gene.
What does a positive result mean?
A positive result confirms the presence of LRRC6 gene mutations, indicating PCD Type 19.
Can the test detect all mutations?
While highly accurate, it may not detect all possible mutations; genetic counseling is advised.
Is genetic counseling required before the test?
Yes, genetic counseling is recommended to understand the test implications and family history.
Which cities offer home collection for this test?
Home collection is available in numerous cities including Mumbai, Delhi, Bangalore, Hyderabad, and many more across India.
How accurate is the NGS test for PCD Type 19?
The NGS test is highly accurate and sensitive for detecting mutations in the LRRC6 gene.
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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