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ARHGDIA Gene Nephrotic syndrome type 8 NGS Genetic Test

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ARHGDIA Gene Nephrotic syndrome type 8 NGS Genetic Test

Short Name: ARHGDIA Gene Test

Also known as: ARHGDIA Gene Mutation Test, Nephrotic Syndrome Type 8 Genetic Test, ARHGDIA NGS Test

ARHGDIA Gene Nephrotic syndrome type 8 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

✍️ Written By

🩺 Medically Reviewed By

Dr SULOCHANA HEMCHANDRA HOLLA

Dr SULOCHANA HEMCHANDRA HOLLA

Consultant Medical Geneticist · Reg: 8532

Last reviewed: September 7, 2026

Overview

The purpose of the ARHGDIA Gene Nephrotic Syndrome Type 8 NGS Genetic Test is to detect mutations in the ARHGDIA gene that cause Nephrotic Syndrome Type 8. This aids in confirming diagnosis, understanding the genetic basis of the disorder, guiding treatment decisions, and facilitating genetic counseling for affected families.

Test Code
2626
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

No specific preparation required. Provide clinical history and undergo genetic counseling.

Method: Venipuncture or blood drop

Step 2

Laboratory Analysis

Blood sample collected via venipuncture or blood drop on FTA card by a trained professional.

Step 3

Report Delivery

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

Timeline: 3 to 4 weeks

Patient Instructions

1
Before the Test:Provide detailed clinical history and family pedigree during genetic counseling.
2
During the Test:Sample collection is quick and minimally invasive, typically taking a few minutes.
3
After the Test:Monitor the puncture site for any discomfort; await results as per the turnaround time.

About This Test

Who Should Get This Test

The purpose of the ARHGDIA Gene Nephrotic Syndrome Type 8 NGS Genetic Test is to detect mutations in the ARHGDIA gene that cause Nephrotic Syndrome Type 8. This aids in confirming diagnosis, understanding the genetic basis of the disorder, guiding treatment decisions, and facilitating genetic counseling for affected families.

How to Prepare

  • Ensure proper identification and labeling of samples
  • Use sterile equipment for blood collection
  • Follow standard phlebotomy procedures
  • Handle FTA cards carefully to avoid contamination

Doctor's Notes

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

"Genetic testing for ARHGDIA gene mutations is essential for accurate diagnosis, personalized treatment, and family counseling in Nephrotic Syndrome Type 8."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Sample Volume5-10 ml blood
ContainerEDTA tube or FTA card
Collection MethodVenipuncture or blood drop

Sample Stability

Blood samples stable for 48 hours at room temperature
Extracted DNA stable for longer periods if stored properly
Sample Rejection Criteria:
  • Hemolyzed or clotted blood samples
  • Insufficient sample volume
  • Improperly labeled or contaminated samples

Understanding Your Results

Results indicate the presence or absence of mutations in the ARHGDIA gene associated with Nephrotic Syndrome Type 8.
Positive result: Pathogenic mutation detected, confirming genetic cause; requires clinical correlation and counseling.
Negative result: No pathogenic mutation detected; does not rule out other genetic or non-genetic causes.
Variant of uncertain significance (VUS): Mutation detected but clinical significance unknown; further testing may be needed.
⚠️ When to Consult a Doctor:

Consult a doctor if symptoms persist, if there is a family history of nephrotic syndrome, or after receiving test results for appropriate management and counseling.

Limitations

  • ⚠May not detect all types of mutations, such as large deletions or duplications
  • ⚠Results require interpretation by a geneticist or healthcare provider
  • ⚠Does not replace clinical evaluation or other diagnostic tests

Risks & Considerations

  • ●Minimal risk from blood draw, such as bruising or infection
  • ●Psychological impact of genetic results; counseling recommended

Interfering Factors

  • ●Sample contamination or degradation
  • ●Insufficient DNA quantity or quality
  • ●Technical errors in sequencing

Compare With Similar Tests

TestARHGDIA Gene Nephrotic syndrome type 8 NGS Genetic TestKidney Function Test (KFT)Renal BiopsyOther Genetic Tests for Nephrotic Syndrome
ComparisonARHGDIA Gene Nephrotic syndrome type 8 NGS Genetic Test

Frequently Asked Questions

What is the ARHGDIA Gene Nephrotic Syndrome Type 8 NGS Genetic Test?
It is a genetic test that uses Next-Generation Sequencing to detect mutations in the ARHGDIA gene, which causes Nephrotic Syndrome Type 8, a rare kidney disorder.
Why is this test important?
It helps diagnose the genetic cause of nephrotic syndrome, guides treatment, and allows for family risk assessment and genetic counseling.
What are the symptoms of Nephrotic Syndrome Type 8?
Symptoms include swelling in legs, ankles, feet, weight gain, foamy urine, fatigue, weakness, and loss of appetite.
How is the test performed?
A blood sample or DNA is collected and analyzed using NGS technology to identify mutations in the ARHGDIA gene.
What is the cost of the test?
The cost is INR 20,000, with free home sample collection available across India.
Is home sample collection available?
Yes, DNA Labs India offers free home sample collection for this test in many cities across India.
How long does it take to get results?
Results are typically available within 3 to 4 weeks after sample collection.
What does a positive result mean?
A positive result indicates a pathogenic mutation in the ARHGDIA gene, confirming the genetic cause of nephrotic syndrome.
What are the risks of the test?
Risks are minimal, such as bruising from blood draw, but genetic results may have psychological impacts; counseling is advised.
Can this test be used for prenatal diagnosis?
Yes, in families with known mutations, it can be used for prenatal or preconception planning after genetic counseling.
How accurate is the test?
NGS technology provides high accuracy for detecting mutations, but results should be interpreted by a genetic specialist.
What should I do after receiving the results?
Consult a healthcare provider or geneticist for interpretation, treatment options, and family 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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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.

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