← Change diagnostic objective
Known gene or documented familial variant
One gene is strongly suspected, but no variant is known
Sequence the gene and confirm dosage coverage.
Clinical test selectorStep 3 of 4
- ✓Clinical scenario
- ✓Diagnostic objective
- 3Available material
- 4Recommendation
STEP 3
What material or documentation is available?
This changes both the preferred test and the practical warning shown in the result.
Original report + new sample
Best for focused confirmation.
Original report only
The scope can be reviewed before collection.
No report is available
Counseling or broader testing may be needed.
Do not collect based on this page alone.
The accepted tube, quantity, quality, pathology information, consent, storage, and shipping conditions must be confirmed for the selected workflow.
