SOHLH1 Gene Oogenesis dysfunction NGS Genetic Test
Short Name: SOHLH1 Gene Test
Also known as: Spermatogenesis and Oogenesis Specific Basic Helix-Loop-Helix 1 Gene Test
SOHLH1 Gene Oogenesis dysfunction 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 SHAILAJA RAGHUNATH MURDESHWAR
Consultant Physician · Reg: 8052
Last reviewed: September 7, 2026
Overview
To identify genetic mutations in the SOHLH1 gene that may cause oogenesis dysfunction, aiding in diagnosis and personalized treatment for reproductive disorders.
- Test Code
- 5542
- 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
Clinical history and genetic counseling session recommended to draw a pedigree chart.
Method: Blood Draw or DNA Extraction
Laboratory Analysis
Standard blood draw procedure or DNA extraction from provided sample.
Report Delivery
Sample is sent to the laboratory for NGS analysis.
Timeline: 3 to 4 Weeks
Patient Instructions
About This Test
Who Should Get This Test
To identify genetic mutations in the SOHLH1 gene that may cause oogenesis dysfunction, aiding in diagnosis and personalized treatment for reproductive disorders.
How to Prepare
- No fasting required
- Bring valid ID and doctor's prescription
- Inform about any medications or supplements
Doctor's Notes
Reviewed by Dr SHAILAJA RAGHUNATH MURDESHWAR — MBBS, MD (General Medicine) · Reg. No. 8052
"Early genetic testing for SOHLH1 mutations can guide personalized treatment for oogenesis dysfunction, improving fertility outcomes."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed or clotted sample
- Insufficient sample volume
- Incorrect labeling or documentation
Understanding Your Results
Pathogenic variant detected
Increased risk of oogenesis dysfunction; consult a genetic counselor for further evaluation and management.
No pathogenic variant detected
Low genetic risk for SOHLH1-related dysfunction; other factors may contribute to symptoms.
If you experience symptoms of oogenesis dysfunction, have a family history of reproductive disorders, or receive abnormal test results.
Limitations
- ⚠May not detect all genetic variants
- ⚠Requires genetic counseling for interpretation
- ⚠Results should be correlated with clinical findings
Risks & Considerations
- ●Minimal risk from blood draw (e.g., bruising, infection)
- ●Psychological impact of genetic results
Interfering Factors
- ●Sample contamination
- ●Degraded DNA
- ●Incorrect sample handling
Compare With Similar Tests
| Test | SOHLH1 Gene Oogenesis dysfunction NGS Genetic Test | AMH Test | FSH Test | Karyotyping | Infertility Gene Panel |
|---|---|---|---|---|---|
| Comparison | SOHLH1 Gene Oogenesis dysfunction NGS Genetic Test |
Frequently Asked Questions
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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.
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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