FOXH1 Gene Congenital heart disease and transposition of the great arteries NGS Genetic Test
Short Name: FOXH1 Gene CHD TGA NGS Test
FOXH1 Gene Congenital heart disease and transposition of the great arteries NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses Next-Generation Sequencing (NGS) 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 FOXH1 Gene NGS Genetic Test is to detect mutations in the FOXH1 gene that are associated with congenital heart disease and transposition of the great arteries. This test helps in confirming diagnosis, guiding treatment decisions, and providing genetic counseling for affected families.
- Test Code
- 5730
- 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
- Next-Generation Sequencing (NGS)
Sample Collection
Provide clinical history of the patient and undergo a genetic counseling session to draw a pedigree chart of family members affected with congenital heart disease.
Laboratory Analysis
Standard blood draw or collection of DNA sample as per instructions.
Report Delivery
Sample is processed and analyzed using NGS technology; results are available in 3 to 4 weeks.
Timeline: 3 to 4 Weeks
Patient Instructions
About This Test
Who Should Get This Test
The purpose of the FOXH1 Gene NGS Genetic Test is to detect mutations in the FOXH1 gene that are associated with congenital heart disease and transposition of the great arteries. This test helps in confirming diagnosis, guiding treatment decisions, and providing genetic counseling for affected families.
How to Prepare
- Blood sample via venipuncture
- Extracted DNA sample
- One drop blood on FTA card
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"Genetic testing for FOXH1 gene mutations is crucial for early detection and management of congenital heart defects, especially in families with a history of heart disease."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Understanding Your Results
Normal
No pathogenic variants detected in the FOXH1 gene.
Pathogenic Variant
Mutation identified; associated with increased risk of congenital heart disease and TGA. Consult a geneticist for management.
Consult a doctor if you or your child experience symptoms such as cyanosis, shortness of breath, or poor growth, or if there is a family history of congenital heart disease.
Limitations
- ⚠May not detect all genetic variants
- ⚠Requires genetic counseling for interpretation
Risks & Considerations
- ●Minimal risk from blood draw, such as bruising or infection
Interfering Factors
- ●Sample contamination
- ●Degraded DNA
Frequently Asked Questions
What is the FOXH1 Gene NGS Genetic Test?
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₹20,000Reference 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.
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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