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.
🩺 Medically Reviewed By
Dr SULOCHANA HEMCHANDRA HOLLA
Consultant Medical Geneticist · Reg: 8532
Last reviewed: September 7, 2026
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
Sample Collection
Provide clinical history and undergo genetic counseling session to draw a pedigree chart.
Method: Venipuncture or FTA Card
Laboratory Analysis
Blood sample will be collected via venipuncture or a single drop on FTA card.
Report Delivery
Apply pressure to the puncture site; samples are processed in the lab.
Timeline: 3 to 4 Weeks
Patient Instructions
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 Dr SULOCHANA HEMCHANDRA HOLLA — 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 Stability
- Hemolyzed or lipemic samples
- Insufficient sample volume
- Incorrectly labeled samples
Understanding Your Results
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
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
| Test | SLC22A12 Gene Hypouricemia, renal type 1 NGS Genetic Test | Uric Acid Blood Test | Kidney Function Panel | Whole Exome Sequencing |
|---|---|---|---|---|
| Comparison | SLC22A12 Gene Hypouricemia, renal type 1 NGS Genetic Test | Measures 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
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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.
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✓ 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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