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ROR2 Gene Brachydactyly type B1 NGS Genetic Test

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ROR2 Gene Brachydactyly type B1 NGS Genetic Test

Short Name: ROR2 Brachydactyly B1 NGS Test

Also known as: Brachydactyly Type B1, ROR2-Related Brachydactyly

ROR2 Gene Brachydactyly type B1 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.

NGS Genetic TestPediatric🏠 Home Collection

🩺 Medically Reviewed By

Overview

To identify pathogenic mutations in the ROR2 gene for diagnosis of brachydactyly type B1 and to guide clinical management.

Test Code
5685
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

Genetic counseling recommended. Provide clinical history and family pedigree.

Method: Venipuncture or FTA card spotting

Step 2

Laboratory Analysis

Blood sample collected via venipuncture or FTA card.

Step 3

Report Delivery

Sample sent to lab for NGS analysis.

Timeline: 3 to 4 weeks

Patient Instructions

1
Before the Test:Consult with a geneticist for counseling and test indication.
2
During the Test:Sample collection and processing.
3
After the Test:Report generation and genetic counseling session.

About This Test

Who Should Get This Test

To identify pathogenic mutations in the ROR2 gene for diagnosis of brachydactyly type B1 and to guide clinical management.

How to Prepare

  • Ensure proper labeling
  • Use sterile equipment
  • Follow aseptic techniques

Doctor's Notes

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

"This NGS test is essential for confirming ROR2 gene mutations, aiding in precise diagnosis and personalized management of brachydactyly type B1."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Sample Volume3-5 ml blood or as required
ContainerEDTA tube or FTA card
Collection MethodVenipuncture or FTA card spotting

Sample Stability

Blood: 24 hours at room temperature
FTA card: stable for extended periods
Sample Rejection Criteria:
  • Hemolyzed samples
  • Insufficient volume
  • Improperly labeled samples

Understanding Your Results

Results indicate the presence or absence of pathogenic variants in the ROR2 gene.
📊

Pathogenic variant detected

Confirms diagnosis of brachydactyly type B1

📊

No pathogenic variant detected

Reduces likelihood, but clinical correlation needed

⚠️ When to Consult a Doctor:

If symptoms of brachydactyly are present or if there is a family history of the condition.

Limitations

  • May not detect all types of mutations
  • Requires genetic counseling for interpretation
  • Results may have implications for family members

Risks & Considerations

  • Minor bruising at blood draw site
  • Rare infection risk

Interfering Factors

  • Sample contamination
  • Degraded DNA
  • Incorrect sample handling

Compare With Similar Tests

TestROR2 Gene Brachydactyly type B1 NGS Genetic TestSanger SequencingClinical Examination
ComparisonROR2 Gene Brachydactyly type B1 NGS Genetic Test

Frequently Asked Questions

What is ROR2 Gene Brachydactyly Type B1?
It is a rare genetic disorder causing short fingers and toes due to mutations in the ROR2 gene.
How is the test performed?
Using Next Generation Sequencing (NGS) on a blood or DNA sample to detect ROR2 gene mutations.
What is the cost of the test?
The test costs INR 20,000 in India, with home collection available.
Is home sample collection available?
Yes, free home collection is offered for online bookings across India.
How long does it take to get results?
Results are typically available in 3 to 4 weeks.
What are the symptoms of brachydactyly type B1?
Symptoms include short, curved, or missing bones in fingers and toes, and difficulty using hands or feet.
How is brachydactyly type B1 diagnosed?
Diagnosis involves physical exam, medical history, and genetic testing like this NGS test.
What is the treatment for this condition?
Treatment may include physical therapy, assistive devices, or surgery to improve function.
Is genetic counseling recommended?
Yes, genetic counseling is advised before and after testing to understand implications.
Can this test be used for prenatal diagnosis?
Consult a geneticist; prenatal testing may be possible in some cases.
What if the test result is negative?
A negative result reduces likelihood, but clinical evaluation is still needed for diagnosis.
How accurate is the NGS genetic test?
NGS is highly accurate for detecting mutations, but interpretation requires expert genetic counseling.
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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