Casandra
Casandra Test Code PG76189Version 1 (DRAFT)
Performing Lab
Bleeding Disorders Panel
Clinical Use
Order TestUse
This test is designed for individuals with relevant clinical features who have a diagnosed or suspected inherited bleeding disorder. It serves to identify genetic variants associated with bleeding diatheses, aiding in the confirmation of the diagnosis and potentially guiding treatment decisions.
Special Instructions
Not provided.
Limitations
The test analyzes 85 genes associated with various bleeding disorders, identifying sequence variants and copy number changes. However, it may not detect all genetic variants responsible for such disorders, especially those outside the tested gene set or within regions poorly covered by the sequencing technology.
Test Details
New York Approved
Methodology
NGS (CGP)
Biomarkers
No genes
GeneSNV/Indel
Mutation • Categorical (e.g., Positive / Negative / Indeterminate)
Result Turnaround Time
14-21 days
Related Documents
For more information, please review the documents below
Specimen Requirements
Specimen
Whole Blood
Volume
Not provided
Minimum Volume
Not provided