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GNA11 Gene Hypocalcemia, autosomal dominant 2 NGS Genetic Test

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GNA11 Gene Hypocalcemia, autosomal dominant 2 NGS Genetic Test

Short Name: GNA11 Hypocalcemia NGS Test

Also known as: GNA11-related hypocalcemia, Autosomal dominant hypocalcemia type 2

GNA11 Gene Hypocalcemia, autosomal dominant 2 NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses NGS Technology 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 Test🏠 Home Collection

🩺 Medically Reviewed By

Overview

To diagnose GNA11 Gene Hypocalcemia, Autosomal Dominant 2 through genetic analysis.

Test Code
4707
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
NGS Technology
Step 1

Sample Collection

Genetic counseling recommended.

Method: Venipuncture

Step 2

Laboratory Analysis

Blood sample collected via venipuncture.

Step 3

Report Delivery

Sample sent to lab for analysis.

Timeline: 3 to 4 weeks

Patient Instructions

1
Before the Test:Consult with a genetic counselor.
2
During the Test:Sample collection and processing.
3
After the Test:Report generation and consultation.

About This Test

Who Should Get This Test

To diagnose GNA11 Gene Hypocalcemia, Autosomal Dominant 2 through genetic analysis.

How to Prepare

  • Ensure proper sample labeling
  • Avoid hemolysis

Doctor's Notes

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

"Genetic testing is crucial for accurate diagnosis and management of hereditary hypocalcemia."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Sample Volume5 ml blood
ContainerEDTA tube or FTA Card
Collection MethodVenipuncture

Sample Stability

Blood sample stable for 48 hours at room temperature
Extracted DNA stable for longer periods
Sample Rejection Criteria:
  • Insufficient sample volume
  • Contaminated sample

Understanding Your Results

Results indicate the presence or absence of mutations in the GNA11 gene.
Positive for mutation: Confirms diagnosis
Negative for mutation: Rules out GNA11-related hypocalcemia
Variant of uncertain significance: Requires further evaluation
⚠️ When to Consult a Doctor:

If symptoms persist or if there is a family history of hypocalcemia.

Limitations

  • May not detect all mutations
  • Requires genetic counseling for interpretation

Risks & Considerations

  • Minimal risk from blood draw
  • Psychological impact of genetic results

Interfering Factors

  • Sample contamination
  • Degraded DNA

Compare With Similar Tests

TestGNA11 Gene Hypocalcemia, autosomal dominant 2 NGS Genetic Test
ComparisonGNA11 Gene Hypocalcemia, autosomal dominant 2 NGS Genetic Test

Frequently Asked Questions

What is GNA11 Gene Hypocalcemia, Autosomal Dominant 2?
It is a rare genetic disorder caused by mutations in the GNA11 gene, leading to low calcium levels in the blood.
What are the symptoms of this disorder?
Symptoms include weakness, fatigue, muscle cramps, tingling, seizures, and abnormal heart rhythms.
How is the disorder diagnosed?
Diagnosis involves physical exams, blood tests, and genetic testing like the NGS Genetic Test.
What is the NGS Genetic Test?
It uses next-generation sequencing to analyze DNA for mutations in the GNA11 gene.
What is the cost of the test in India?
The test costs INR 20,000 at DNA Labs India.
Is home sample collection available?
Yes, free home collection is available in many cities across India.
How long does it take to get results?
Results are typically available in 3 to 4 weeks.
What sample is required for the test?
Blood, extracted DNA, or one drop blood on FTA card.
Is fasting required before the test?
No, fasting is not required.
What if the test result is positive?
A positive result confirms the diagnosis, and a doctor can recommend appropriate treatment.
Can children undergo this test?
Yes, the test is suitable for all ages.
How accurate is the test?
The test is highly accurate for detecting mutations in the GNA11 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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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.

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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.

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