P2RY12 Gene Bleeding disorder, platelet-type 8 NGS Genetic Test
Short Name: P2RY12 Gene Test
Also known as: Platelet-type 8 bleeding disorder, P2RY12-related bleeding disorder, Inherited platelet dysfunction
P2RY12 Gene Bleeding disorder, platelet-type 8 NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses NGS (Next-Generation Sequencing) 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 mutations in the P2RY12 gene for diagnosis of platelet-type 8 bleeding disorder, aiding in clinical management and genetic counseling.
- Test Code
- 2655
- 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 (Next-Generation Sequencing)
Sample Collection
Clinical history of the patient and a genetic counseling session to draw a pedigree chart of family members affected with P2RY12 gene bleeding disorder.
Method: Venipuncture or FTA card collection
Laboratory Analysis
Standard blood draw or FTA card collection procedure.
Report Delivery
Apply pressure to the puncture site to prevent bruising.
Timeline: 3 to 4 Weeks
Patient Instructions
About This Test
Who Should Get This Test
To identify mutations in the P2RY12 gene for diagnosis of platelet-type 8 bleeding disorder, aiding in clinical management and genetic counseling.
How to Prepare
- Use blood, extracted DNA, or one drop blood on FTA card
- Ensure proper labeling and handling
Doctor's Notes
Reviewed by Dr SHAILAJA RAGHUNATH MURDESHWAR — MBBS, MD (General Medicine) · Reg. No. 8052
"This test is essential for diagnosing inherited bleeding disorders like platelet-type 8, enabling personalized management and genetic counseling for affected families."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Understanding Your Results
Mutation detected
Diagnosis of P2RY12 gene bleeding disorder confirmed; genetic counseling recommended.
No mutation detected
Disorder unlikely, but clinical correlation is advised if symptoms persist.
If you experience symptoms of bleeding disorders such as easy bruising, prolonged bleeding, or have a family history of such conditions.
Limitations
- ⚠Only detects mutations in the P2RY12 gene
- ⚠May not identify all genetic variants
Risks & Considerations
- ●Minor bruising at puncture site
- ●Rare risk of infection
Interfering Factors
- ●Sample contamination
- ●Improper sample storage
Frequently Asked Questions
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