FANCC Gene Fanconi anemia type C NGS Genetic Test
Short Name: FANCC Gene Test
Also known as: FANCC Mutation Analysis, Fanconi Anemia Type C DNA Test, FANCC Gene Sequencing
FANCC Gene Fanconi anemia type C 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 this test is to identify pathogenic mutations in the FANCC gene to diagnose Fanconi Anemia Type C, assess carrier status in family members, and inform treatment strategies and genetic counseling.
- Test Code
- 1981
- Price
- ₹20,000
- Sample Type
- Blood or Extracted DNA or One drop Blood on FTA Card
- Result Time
- 3 to 4 weeks
- Fasting Required
- Yes
- Method
- Next Generation Sequencing (NGS)
Sample Collection
Fast for 8-12 hours before blood sample collection. Provide a detailed clinical history and family pedigree if available.
Method: Venipuncture
Laboratory Analysis
A blood sample will be collected via venipuncture by a trained phlebotomist or healthcare professional.
Report Delivery
Apply pressure to the puncture site to prevent bleeding or bruising. Resume normal activities unless advised otherwise.
Timeline: 3 to 4 weeks
Patient Instructions
About This Test
Who Should Get This Test
The purpose of this test is to identify pathogenic mutations in the FANCC gene to diagnose Fanconi Anemia Type C, assess carrier status in family members, and inform treatment strategies and genetic counseling.
How to Prepare
- Fast for 8-12 hours prior to the test
- Bring a valid ID and doctor's prescription or referral
- Inform the collection technician about any medications, health conditions, or allergies
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"This genetic test is crucial for confirming Fanconi Anemia Type C, enabling early intervention and family planning counseling, especially in cases with a family history or suggestive symptoms."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed or clotted sample
- Incorrect sample type or container
- Insufficient sample volume
- Leaking or damaged sample tube
Understanding Your Results
Negative
No pathogenic variants detected in the FANCC gene. Clinical correlation is advised, as symptoms may be due to other causes.
Positive
Pathogenic variant(s) identified in the FANCC gene, confirming a diagnosis of Fanconi Anemia Type C. Genetic counseling and further clinical evaluation are recommended.
If you exhibit symptoms of Fanconi Anemia, have a family history of the disorder, or receive a positive test result, consult a healthcare professional promptly for diagnosis and management.
Limitations
- ⚠May not detect all types of genetic variants, such as large deletions or deep intronic mutations
- ⚠Requires confirmation with additional tests (e.g., Sanger sequencing) in some cases
- ⚠Genetic counseling is recommended before and after testing to interpret results
Risks & Considerations
- ●Minimal risk from blood draw, such as bruising, swelling, or infection at the puncture site
- ●Rare risk of fainting or dizziness during venipuncture
Interfering Factors
- ●Poor sample quality (e.g., hemolyzed or clotted blood)
- ●Contamination during sample collection or processing
- ●Insufficient DNA quantity or quality
Compare With Similar Tests
| Test | FANCC Gene Fanconi anemia type C NGS Genetic Test | ||
|---|---|---|---|
| Comparison | FANCC Gene Fanconi anemia type C NGS Genetic Test | Detects chromosomal instability but is less specific for individual gene mutations; often used as an initial screening test. | Traditional sequencing method with lower throughput and higher cost per gene compared to NGS; suitable for confirming specific variants. |
Frequently Asked Questions
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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.
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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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