Provider-ordered panels through our lab partner PreCheckHealth Services: pharmacogenomics, hereditary cancer, immunogenetics, and neurogenetics. The patient ships a kit, PreCheckHealth bills insurance directly, and your clinic adds molecular depth without standing up a lab line. Clinical diagnostics, not consumer SNP testing.
TITN does not run a genetics lab and does not resell tests. We refer to PreCheckHealth Services, a clinical laboratory, so your functional and longevity patients can add molecular depth. You order, the patient ships the kit, and PreCheckHealth bills insurance directly.
#10D2210020 · CAP #9101993. Certified under CLIA 1988 to perform high-complexity molecular testing, both numbers as published by PreCheckHealth Services.
Coverage and patient responsibility vary by payer, plan, and panel. Confirm specifics with PreCheckHealth before ordering.
PharmacoCheck+ and the Comprehensive Neurogenetic Panel lead, because they pair cleanly with what TITN already does: medication metabolism for ALTMS, and genetic predisposition alongside WAVi brain function. CancerCheck and ImmunoCheck sit adjacent for the practices that need them.
Drug-metabolizing enzyme variants that inform medication selection and dosing. Where a patient sits on the metabolizer spectrum can change which drug, and which dose, makes sense before the first prescription.
A 203-gene neurogenetic panel for genetic predisposition across neurological presentations. Read alongside a WAVi scan, it puts genetic risk next to functional brain measurement: the predisposition and the present-day picture together.
A 116-gene hereditary cancer panel for patients whose history or risk profile warrants a structured look at inherited cancer-predisposition genes. Provider-ordered, with counseling to support how results are delivered.
A 291-gene immunogenetic panel for patients whose immune-related questions benefit from a genetic lens: inborn errors of immunity, autoimmune predisposition, and immunotherapy responsiveness. Same provider-ordered workflow as the other three.
No lab to stand up, no specimen pickup to manage, no genetics billing to learn. The workflow keeps your clinic focused on the clinical question.
The ordering provider selects the appropriate panel for a clinical question, the same way any provider-ordered test is initiated.
The patient receives a collection kit and ships the sample back to PreCheckHealth. No in-clinic specimen handling required.
PreCheckHealth bills the patient's insurance directly for the panel. The clinic does not bill, and TITN does not bill.
Clinical results return to the ordering provider, with virtual genetic counseling available to support interpretation and patient delivery.
Provider-ordered genetics is most useful where it answers a question the patient is already asking: why a medication worked or did not, where inherited risk sits, and how predisposition lines up with present-day function.
PharmacoCheck+ surfaces drug-metabolizing enzyme variants so prescribing starts informed, not by trial and error. Especially relevant for psychiatric medication metabolism.
The 203-gene Comprehensive Neurogenetic Panel adds inherited-risk context. Read with a WAVi scan, predisposition and functional brain data sit side by side.
CancerCheck (116 genes) gives a structured look at inherited cancer-predisposition genes for patients whose history warrants it, with counseling on delivery.
ImmunoCheck (291 genes) brings a genetic lens to immune-related questions, ordered through the same provider workflow as the other panels.
For functional-medicine and longevity patients who want more than a snapshot, genetics adds a durable molecular layer to the workup.
Virtual genetic counseling helps the ordering provider deliver results responsibly, so a complex finding lands with context, not anxiety.
Genetics is only useful if the read is responsible. Provider-ordered panels return to the ordering provider, and virtual genetic counseling is available so the conversation with the patient is supported. Where TITN's own diagnostics overlap, BMTG can frame the genetic layer alongside functional data.
Provider-ordered genetics can surface findings that need careful delivery. Virtual genetic counseling is available through the panel workflow to help the ordering provider interpret and communicate results, so a high-impact finding reaches the patient with context.
For neurogenetic work, the genetic layer is strongest when it sits beside functional brain data. Pair the Comprehensive Neurogenetic Panel with a WAVi scan to put inherited risk and measured brain function in the same workup, with BMTG framing the combined picture where it applies.
The practices that already think in baselines and risk profiles tend to adopt genetics first. Where it lands:
The questions providers ask before they refer for clinical genetic testing.
Yes. The panels are processed by PreCheckHealth, a CLIA and CAP accredited laboratory. This is provider-ordered clinical testing, not consumer SNP testing.
TITN refers; PreCheckHealth bills. The laboratory bills insurance directly under a patient-referral model, so the practice does not stand up its own lab or carry the billing.
Four: pharmacogenomics, hereditary cancer risk, immunogenetics, and neurogenetics.
A provider orders the panel, and genetic counseling is available to interpret results. The findings can pair with functional brain data from WAVi for a fuller clinical picture.
No. These are clinical-grade, provider-ordered panels run by an accredited lab, not a direct-to-consumer ancestry or wellness DNA kit.
Book a 15-minute call. We will walk the four panels, the referral workflow, the PreCheckHealth billing model, and how genetics pairs with WAVi and ALTMS for your patients.
Book a 15-min callSpot a broken or outdated link? Email roberto@transitionitnow.com.