Rare Disease Genomics
ExomeDx — Exome Sequencing
AC-GDX-561B · GeneDx
Exome sequencing with interpretation against GeneDx's rare-disease dataset. Available proband-only, duo, or trio (patient plus one or both biological parents), with trio generally improving yield and reducing uncertain results. Holds FDA Breakthrough Device designation.
Order this test
Send the clinical question and specimen details and AC confirms the pathway, collection requirements, and logistics.
Order in the portalNot a client yet? Ask usHow ordering works →Test details
- Test code
- AC-GDX-561B
- Performing lab
- GeneDx
- Clinical area
- Rare Disease Genomics
- Method
- Whole exome sequencing — proband, duo, or trio
- Specimen
- EDTA whole blood or buccal swab
- Turnaround
- ~29 days incl. shipping
Turnaround is quoted end to end — the reference laboratory’s processing time plus courier transit from Jordan, 5 days to Korea and 8 days to the United States. It is indicative, not a guarantee, and may vary with specimen quality and shipment timing.
Sample requirements
Collect EDTA whole blood or buccal swab. Full handling, storage, and stability requirements are confirmed when you order. See sample requirements for general collection guidance.
Other tests in Rare Disease Genomics
For healthcare professionals. Tests are ordered and interpreted in consultation with a qualified physician. Test names are the performing laboratory’s own. Pricing is per-institution and confirmed on request.