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DNA Labs India

SLC22A12 Gene Hypouricemia, renal type 1 NGS Genetic Test

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SLC22A12 Gene Hypouricemia, renal type 1 NGS Genetic Test

Short Name: SLC22A12 Hypouricemia Test

Also known as: Renal Hypouricemia Type 1 Genetic Test, SLC22A12 Gene Sequencing Test

SLC22A12 Gene Hypouricemia, renal type 1 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 TestAll Ages🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of the SLC22A12 Gene Hypouricemia, Renal Type 1 NGS Genetic Test is to identify mutations in the SLC22A12 gene that cause renal hypouricemia. This allows for accurate diagnosis, assessment of disease risk, guidance on management, and family genetic counseling.

Test Code
2120
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

Provide clinical history and undergo genetic counseling session to draw a pedigree chart.

Method: Venipuncture or FTA Card

Step 2

Laboratory Analysis

Blood sample will be collected via venipuncture or a single drop on FTA card.

Step 3

Report Delivery

Apply pressure to the puncture site; samples are processed in the lab.

Timeline: 3 to 4 Weeks

Patient Instructions

1
Before the Test:Genetic counseling and family history assessment are recommended before testing.
2
During the Test:The test involves a simple blood draw; no special procedures are required.
3
After the Test:Results are available in 3-4 weeks; genetic counseling is provided for interpretation.

About This Test

Who Should Get This Test

The purpose of the SLC22A12 Gene Hypouricemia, Renal Type 1 NGS Genetic Test is to identify mutations in the SLC22A12 gene that cause renal hypouricemia. This allows for accurate diagnosis, assessment of disease risk, guidance on management, and family genetic counseling.

How to Prepare

  • Ensure patient is comfortable and relaxed.
  • Use aseptic techniques for blood collection.
  • Label samples correctly with patient details.

Doctor's Notes

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

"Genetic testing for SLC22A12 gene mutations is crucial for diagnosing renal hypouricemia, enabling personalized management and family counseling."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Collection MethodVenipuncture or FTA Card

Sample Stability

Blood: 24 hours at room temperature
Extracted DNA: Stable for years at -20°C
Sample Rejection Criteria:
  • Hemolyzed or lipemic samples
  • Insufficient sample volume
  • Incorrectly labeled samples

Understanding Your Results

The test results indicate the presence or absence of mutations in the SLC22A12 gene. A positive result confirms a genetic cause for renal hypouricemia, while a negative result may suggest other etiologies.
📊

Confirms diagnosis of SLC22A12 Gene Hypouricemia, Renal Type 1. Genetic counseling and management planning recommended.

High

📊

Further testing or family studies may be needed. Clinical correlation is advised.

Moderate

📊

SLC22A12 gene mutation unlikely. Consider other causes of hypouricemia.

Low

⚠️ When to Consult a Doctor:

Consult a doctor if you experience symptoms like recurrent kidney stones, chronic kidney disease, or if there is a family history of renal hypouricemia. Genetic counseling is recommended post-test.

Limitations

  • May not detect all possible genetic variants
  • Results require clinical correlation
  • Does not assess other causes of hypouricemia

Risks & Considerations

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

Interfering Factors

  • Contaminated DNA sample
  • Recent blood transfusion
  • Improper sample storage

Compare With Similar Tests

TestSLC22A12 Gene Hypouricemia, renal type 1 NGS Genetic TestUric Acid Blood TestKidney Function PanelWhole Exome Sequencing
ComparisonSLC22A12 Gene Hypouricemia, renal type 1 NGS Genetic TestMeasures uric acid levels but does not identify genetic causes.Assesses overall kidney health but not specific genetic mutations.Broader genetic analysis, more costly, used for multiple conditions.

Frequently Asked Questions

What is SLC22A12 Gene Hypouricemia, Renal Type 1?
It is a genetic condition caused by mutations in the SLC22A12 gene, leading to low uric acid levels and kidney-related symptoms due to impaired uric acid transport.
What are the common symptoms of this condition?
Symptoms include recurrent kidney stones, chronic kidney disease, abnormal urine color, abdominal pain, joint pain, gout attacks, and high blood pressure.
How is the diagnosis confirmed?
Diagnosis is confirmed through NGS genetic testing of the SLC22A12 gene, which detects specific mutations causing the condition.
What is the cost of the test at DNA Labs India?
The test costs INR 20000, which includes genetic counseling and result interpretation.
Is home sample collection available?
Yes, free home sample collection is offered for online bookings across numerous cities in India.
How long does it take to get the results?
Results are typically available within 3 to 4 weeks after sample collection.
What sample type is required for the test?
The test can be performed using blood, extracted DNA, or one drop of blood on an FTA card.
Is fasting required before the test?
No, fasting is not required for this genetic test.
Who should consider getting this test?
Individuals with symptoms of renal hypouricemia, a family history of the condition, or those seeking genetic diagnosis should consider this test.
What does a positive test result mean?
A positive result confirms a genetic mutation in the SLC22A12 gene, indicating a higher risk for renal hypouricemia and related complications.
Are there any risks associated with the test?
The risks are minimal, primarily related to blood draw, such as bruising. Genetic results may have psychological implications, which are addressed through counseling.
How can I schedule the test?
You can schedule the test online through DNA Labs India's website or by contacting their customer service for assistance.
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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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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