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.
🩺 Medically Reviewed By
Dr SULOCHANA HEMCHANDRA HOLLA
Consultant Medical Geneticist · Reg: 8532
Last reviewed: September 7, 2026
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)
Sample Collection
Provide clinical history and undergo genetic counseling if recommended.
Method: Venipuncture or FTA card collection
Laboratory Analysis
Blood sample collected via venipuncture or FTA card as per standard procedure.
Report Delivery
Sample is labeled and sent to the laboratory for analysis.
Timeline: 3 to 4 weeks
Patient Instructions
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 Dr SULOCHANA HEMCHANDRA HOLLA — 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 Stability
- Hemolyzed sample
- Insufficient volume
- Improper labeling
- Contaminated sample
Understanding Your Results
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.
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
| Test | LRRC6 Gene Primary ciliary dyskinesia type 19 NGS Genetic Test | PCD Panel NGS Test | Sanger Sequencing for LRRC6 |
|---|---|---|---|
| Comparison | LRRC6 Gene Primary ciliary dyskinesia type 19 NGS Genetic Test |
Frequently Asked Questions
What is the LRRC6 Gene PCD Type 19 NGS Genetic Test?
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Is home sample collection available?
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