Genetics: Counseling, Testing, Screening
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Coverage criteria for genetic counseling, testing, and screening services for Priority Health members, including medical necessity, prior authorization, and services managed through eviCore. Applies to providers ordering or performing genetic services for affected members.
No material clinical or coverage changes in this revision.
Coverage Criteria
I. MEDICAL NECESSITY CRITERIA
Genetic counseling, testing and prenatal genetic services — Coverage is determined by the following medical necessity criteria and exclusions.
Counseling must be performed by a board-certified genetic counselor independent of the testing laboratory for specified conditions (see Appendix A). Counseling may occur at the same visit as sample collection with documentation.
Michigan law requires informed consent for predictive genetic testing (Public Health Code Act 368 of 1978: Sec. 333.17020).
Selected tests require prior authorization via Evicore. See Section VI (Coding) and Evicore guidelines via Priority Health Prism -> Authorizations -> Authorization Criteria Lookup.
Tumor chemoresistance/chemosensitivity assays
- Tumor in vitro chemoresistance and chemosensitivity assays are considered experimental, investigational, and not medically necessary for brain tumors/brain metastases (eg, 3D Predict Glioma).
- Tumor in vitro chemoresistance and chemosensitivity assays are considered experimental, investigational, and not medically necessary for breast cancer (eg, Theralink Reverse Phase Protein Array).
- Other in vitro chemoresistance/chemosensitivity assays are vendor-managed via Evicore.
Refer prior authorization to Evicore for determination.
General coverage statements
- Genetic carrier screening, gene expression analysis, predictive genetic testing, pharmacogenomic testing, prognostic testing, and diagnostic testing for suspected genetic conditions may be medically necessary according to Evicore guidelines.
- Whole genome sequencing (WGS), whole exome sequencing (WES), mitochondrial whole genome analysis, and genome-wide association studies conducted in the outpatient setting may be medically necessary per Evicore.
E. Prenatal Testing
Prenatal testing, NIPT, diagnostic invasive testing, rWGS and selected prenatal-related exclusions and conditions.
ALL of the following
- Appropriate education and genetic counseling occurs prior to testing.
- Pregnancy is singleton or twin.
- Gestational age is within the testing laboratory's validated window.
M. Rapid Whole Genome Sequencing (rWGS)
Rapid Whole Genome Sequencing (rWGS) — inpatient pediatric use criteria and notification requirement.
ALL of the following
- Ordered after determination by a Board-Certified or Board-Eligible Medical Geneticist that testing could be useful in establishing a diagnosis and treatment options.
- Member is less than 18 years of age.
Clinical timing
- Tested within 1 week of admission to the hospital.
- Tested within 1 week of development of an abnormal response to standard therapy for an underlying condition.
inv-165: Per-code / Per-test Coverage and Dispositions
Per-code and per-test coverage dispositions and prior authorization (eC PA) requirements. The following summarizes representative CPT, HCPCS, and U-code tests with their coverage category and any specific conditions.
Per-code coverage actions and conditions
- Codes designated 'eC PA' require electronic prior authorization via the eC/ Evicore process before testing is performed.
- Codes designated 'No PA required' or 'OOS for eC - No PA required' do not require prior authorization but remain subject to medical necessity documentation and any line-of-business limitations.
- Codes designated 'Not Covered' are considered not medically necessary and should not be billed for those lines of business; see per-code listing for applicable codes and any diagnosis limitations (eg, bladder tumor markers covered only for specified bladder neoplasm ICD-10 codes).
Coverage dispositions (examples)
- Select U-codes for complex genomic tests, tumor profiling, transplant dd-cfDNA, pharmacogenomic panels, and MRD assays (eg, 0072U-0074U, 0088U, 0094U, 0118U, 0239U, 0242U, 0244U, 0246U, 0239U, 0306U-0307U, 0326U, 0327U, 0379U, 0388U, 0391U, 0473U-0475U, 0477U, 0481U, 0561U-0562U, etc.) are identified as eC PA. Some U-codes are explicitly Not Covered (eg, 0248U, 0249U, 0295U, 0301U, 0302U, 0295U).
Per-test coverage categories and special conditions
- When coverage is limited to specific diagnoses, the relevant ICD-10 codes must be present on the claim (eg, bladder antigen tests).
inv-166/167/168/169/170: Gene-specific Panels, Minimal Gene Sets, and eC PA vs Not Covered Stances
Gene-specific, panel-specific and specialty-area coverage stances including minimal gene set expectations and eC PA vs Not Covered distinctions.
Gene/panel coverage stance
- Disease- or phenotype-specific panels (eg, cardiac ion channelopathies 81413/81414, epilepsy 81419, hearing loss 81430/81431, hereditary breast/ovarian 81432/0129U/0102U, hereditary colon cancer 81435/0101U/0102U, inherited cardiomyopathy 81439, nuclear-encoded mitochondrial gene panel 81440, IBMFS 81441, Noonan spectrum 81442) are generally designated eC PA; panels must meet minimal gene-set composition defined in the code description.
Coverage stance (eC PA vs Not Covered)
- Codes marked eC PA: prior authorization required electronically; coverage approval depends on documentation of medical necessity per Evicore criteria and the specific clinical context.
- Codes/Tests marked Not Covered: deemed experimental/investigational or not medically necessary for indicated uses and should not be billed; examples include certain infectious NGS assays, some niche U-codes, and tumor chemoresistance assays (see table).
- Codes with 'Review in panels' status are evaluated in the context of a panel and may require eC PA or medical review prior to payment.
Coding and Test Codes
| 81234 | DMPK (DM1 protein kinase) gene analysis; evaluation to detect abnormal (expanded) alleles |
| 81235 | EGFR gene analysis, common variants (eg, exon 19 LREA deletion, L858R, T790M, G719A, G719S, L861Q) |
| 81236 | EZH2 gene analysis, full gene sequence |
| 81237 | EZH2 gene analysis, common variant(s) (eg, codon 646) |
| 81238 | F9 (coagulation factor IX) full gene sequence |
| 81239 | DMPK gene analysis; characterization of alleles (eg, expanded size) |
| 81240 | F2 (prothrombin) gene analysis, 20210G>A variant |
| 81241 | F5 (Factor V) gene analysis, Leiden variant |
| 81242 | FANCC gene analysis, common variant (eg, IVS4+4A>T) |
| 81243 | FMR1 gene analysis; evaluation to detect abnormal (eg, expanded) alleles |
| 81302 | MECP2 gene analysis; full sequence analysis |
| 81303 | MECP2 known familial variant |
| 81304 | MECP2 duplication/deletion variants |
| 81305 | MYD88 p.Leu265Pro (L265P) variant |
| 81306 | NUDT15 gene analysis, common variant(s) |
| 81307 | PALB2 full gene sequence |
| 81308 | PALB2 known familial variant |
| 81309 | PIK3CA targeted sequence analysis (eg, exons 7,9,20) |
| 81310 | NPM1 exon 12 variants |
| 81311 | NRAS gene analysis, variants in exon 2 and 3 |
| 81400 | Molecular pathology procedure, Level 1 |
| 81401 | Molecular pathology procedure, Level 2 |
| 81402 | Molecular pathology procedure, Level 3 |
| 81403 | Molecular pathology procedure, Level 4 |
| 81404 | Molecular pathology procedure, Level 5 |
| 81405 | Molecular pathology procedure, Level 6 |
| 81406 | Molecular pathology procedure, Level 7 |
| 81407 | Molecular pathology procedure, Level 8 |
| 81408 | Molecular pathology procedure, Level 9 |
| 81411 | Aortic dysfunction duplication/deletion analysis panel |
| 81464 | Solid organ neoplasm, cfDNA panel with comprehensive analysis (DNA/RNA, CNV, MSI, TMB, rearrangements) |
| 81465 | Whole mitochondrial genome large deletion analysis panel |
| 81470 | X-linked intellectual disability (XLID) panel |
| 81490 | (Code referenced in list) |
| 81493 | Coronary artery disease, mRNA, gene expression profiling of 23 genes |
| 81500 | Oncology (ovarian), biochemical assays of two proteins (CA-125 and HE4) with algorithm |
| 81503 | Oncology (ovarian), biochemical assays of five proteins with algorithm |
| 81504 | Oncology (tissue of origin), microarray gene expression profiling >2000 genes |
| 81507 | Fetal aneuploidy DNA sequence analysis of selected regions using maternal plasma |
| 81508 | Fetal congenital abnormalities, biochemical assays of two proteins (PAPP-A, hCG) |
| 0002M | (PLA/Mol test code) |
| 0003M | (PLA/Mol test code) |
| 0004M | (PLA/Mol test code) |
| 0006M | (PLA/Mol test code) |
| 0007M | (PLA/Mol test code) |
| 0001U | (PLA/Proprietary test code) |
| 0018U | (PLA/Proprietary test code) |
| 0019U | (PLA/Proprietary test code) |
| 0022U | (PLA/Proprietary test code) |
| 0023U | (PLA/Proprietary test code) |
| 0239U | Targeted genomic sequence analysis panel, solid organ neoplasm, cell-free DNA, 311+ genes (FoundationOne Liquid CDx) |
| 0242U | Targeted genomic sequence analysis panel, cfDNA 55-74 genes (Guardant360 CDx) |
| 0260U | Identification of CNVs by optical genome mapping |
| 0262U | Oncology gene expression profiling by RT-PCR of 7 gene pathways |
| 0264U | Optical genome mapping (Praxis) |
| 0265U | Whole genome and mitochondrial DNA sequence analysis (Praxis Whole Genome) |
| 0266U | Tissue-specific gene expression by whole-transcriptome |
| 0267U | Optical genome mapping and whole genome sequencing combined |
| 0268U | Hematology aHUS genomic sequence analysis of 15 genes |
| 0269U | Autosomal dominant congenital thrombocytopenia genomic sequence analysis of 14 genes |
| 0407U | CKD risk algorithm (IntelxDKD) - Not Covered |
| 0409U | Oncology (solid), DNA (80) and RNA (36) NGS from plasma |
| 0411U | Psychiatry genomic analysis panel including CYP2D6 CNV |
| 0477U | Pharmacogenomic genotyping of 14 genes including CYP2D6 CNV |
| 0481U | IDH1, IDH2, and TERT promoter NGS (tumor) |
| 0485U | Cell-free DNA and RNA NGS with interpretative report (Caris Assure) |
| 0486U | Tumor methylation markers in cfDNA (Northstar Response) |
| 0478U | Oncology (NSCLC), digital PCR of 9 genes in FFPE tissue |
| 0485U | Cell-free DNA/RNA NGS with interpretative report |
| 0555U | Genetic PGT-SR Plus embryonic genomic analysis per embryo |
| 0560U | MRD baseline genomic sequence analysis, cfDNA |
| 0561U | MRD subsequent cfDNA assessment |
| 0562U | Targeted cfDNA panel, 33 genes (plasma) |
| 82172 | Apolipoprotein, each |
| 83006 | Growth stimulation expressed gene 2 (ST2) |
| 83950 | Oncoprotein; HER-2/neu |
| 83951 | Oncoprotein; des-gamma-carboxy-prothrombin (DCP) |
| 83993 | Calprotectin, fecal |
| 84233 | Receptor assay; estrogen |
| 84234 | Receptor assay; progesterone |
| 86152 | Cell enumeration using immunologic selection (eg, circulating tumor cells) |
| 86153 | Cell enumeration interpretation and report |
| 86294 | Immunoassay for tumor antigen, qualitative (eg, bladder tumor antigen) |
| 88121 | Cytopathology, in situ hybridization, urinary tract specimen (UroVysion) |
| 88130 | Sex chromatin identification; Barr bodies |
| 88182 | Flow cytometry, cell cycle or DNA analysis |
| 88184 | Flow cytometry, cell surface, technical component; first marker |
| 88185 | Flow cytometry each additional marker |
| 88187 | Flow cytometry interpretation; 2 to 8 markers |
| 88189 | Flow cytometry interpretation; 16 or more markers |
| 88230 | Tissue culture for non-neoplastic disorders; lymphocyte |
| 88233 | Tissue culture for non-neoplastic disorders; skin or other solid tissue biopsy |
| 88235 | Tissue culture for non-neoplastic disorders; amniotic fluid or chorionic villus cells |
| 88241 | Thawing and expansion of frozen cells, each aliquot |
| 88245 | Chromosome analysis for breakage syndromes; baseline SCE, 20-25 cells |
| 88248 | Chromosome analysis for breakage syndromes; baseline breakage, score 50-100 cells |
| 88249 | Chromosome analysis for breakage syndromes; score 100 cells, clastogen stress |
| 88261 | Chromosome analysis; count 5 cells, 1 karyotype |
| 88262 | Chromosome analysis; count 15-20 cells, 2 karyotypes |
| 88263 | Chromosome analysis; count 45 cells for mosaicism |
| 88264 | Chromosome analysis; analyze 20-25 cells |
| 88267 | Chromosome analysis, amniotic fluid or chorionic villus, count 15 cells |
| 88271 | Molecular cytogenetics; DNA probe, each (eg, FISH) |
| 88360 | Morphometric analysis, tumor immunohistochemistry, manual |
| 88361 | Morphometric analysis, tumor immunohistochemistry, computer-assisted |
| 88363 | Examination and selection of retrieved archival tissue(s) for molecular analysis |
| 88364 | In situ hybridization, per specimen; each additional single probe stain |
| 88365 | In situ hybridization, each probe |
| 88366 | In situ hybridization, per specimen; each multiplex probe stain |
| 88367 | Morphometric analysis, ISH, computer-assisted; initial single probe |
| 88368 | Morphometric analysis, ISH, manual, per specimen; each probe |
| 88369 | Morphometric analysis, ISH, manual; each additional single probe |
| 88373 | Morphometric analysis, ISH, computer-assisted; each additional single probe |
Provider Actions and Prior Authorization
Evicore prior authorization required
Selected genetic tests require prior authorization administered through Evicore; providers must obtain prior authorization via the Priority Health Prism Evicore workflow before ordering tests that are designated eC PA. See Section VI (Coding) for specific CPT/PLA codes that require Evicore PA.
- Access Evicore: Priority Health Prism → Authorizations → Authorization Criteria Lookup
Check Evicore PA / panel-review status for listed codes
Many molecular and genetic CPT/PLA codes in the coding tables are designated 'eC PA' or 'Review in panels' and therefore require prior authorization or panel-level review through Evicore when applicable; check each code's line-of‑business disposition before ordering.
Meaning of 'eC PA' and 'Review in panels'
'eC PA' next to a code indicates the payer requires electronic prior authorization through Evicore; codes labeled 'Review in panels' are subject to panel-level review and medical necessity assessment rather than standalone coverage.
Electronic prior authorization or panel review required
Many tests in the tables are labeled 'eC PA' or 'Review in panels' for Commercial, Medicaid, and Priority Medicare; providers must obtain electronic prior authorization or complete the panel review process before performing or billing these services.
Obtain PA before billing eC PA or panel‑review codes
Providers must submit prior authorization via Evicore for CPT/PLA codes that are designated 'eC PA' before billing; orders for codes marked 'Review in panels' should follow panel-review initiation per Evicore guidance.
Summary: many codes require prior authorization
Across the coding tables many CPT and PLA/HCPCS codes are annotated as requiring prior authorization ('eC PA') for the indicated plan types; confirm PA requirements for each code in Section VI prior to ordering.
eC PA required before billing
Tests listed with 'eC PA' require electronic prior authorization through Evicore prior to service and billing; do not bill these services without approved PA for the applicable plan.
Verify PA requirement for listed codes
Numerous codes in the tables are annotated 'eC PA' indicating prior authorization is required; verify and obtain Evicore PA for the specific U/CPT code and member plan before performing the test.
Routine eC PA for many listed tests
Tests in the listed CPT ranges are frequently marked 'eC PA'; providers must request and receive Evicore electronic prior authorization for those tests under the applicable plan prior to testing and billing.
eC PA required for many U‑codes
Many U‑codes in the PLA listings show 'COMMERCIAL PLANS = eC PA; MEDICAID = eC PA; PRIORITY MEDICARE = eC PA' — if the ordered U‑code is so annotated, obtain Evicore electronic clinical prior authorization before service.
Electronic case‑by‑case prior authorization required
Some tests require electronic case‑by‑case prior authorization (eC PA) for coverage under Commercial, Medicaid, and Priority Medicare; providers should submit PA requests through Evicore for these entries prior to service.
PA and evidence review required for PLA/HCPCS tests
PLA/HCPCS-coded tests annotated 'eC PA' are covered only after evidence review and prior authorization; submit Evicore PA and supporting documentation per the code entry before performing the test.
Obtain eC PA for listed PLA/U‑codes
Many PLA/HCPCS and U‑code entries are annotated 'eC PA' indicating electronic clinical prior authorization is required before services are rendered or billed for the listed plans.
U‑codes require eC PA across plans
Multiple U‑codes show 'COMMERCIAL PLANS = eC PA. MEDICAID = eC PA. PRIORITY MEDICARE = eC PA.' — providers must obtain Evicore electronic prior authorization for these U‑codes across plan types prior to testing.
G9143 requires prior authorization
Warfarin responsiveness testing (G9143) is designated eC PA and requires prior authorization through Evicore for Commercial, Medicaid, and Priority Medicare before service.
Obtain informed consent and document genetic counseling
Documented informed consent must occur before testing and pre‑ and post‑test genetic counseling must be provided and documented; for specified conditions counseling must be by a board‑certified genetic counselor independent of the testing laboratory.
- Counseling may occur at same visit if documentation meets requirements
- Michigan informed consent law applies (Mich. Comp. Laws 333.17020)
Include medical necessity and counseling documentation with PA/claims
When submitting authorization or claims, include documentation supporting medical necessity (diagnosis, clinical rationale) and document genetic counseling; CPT/HCPCS counseling codes 96041 and S0265 are available when criteria are met.
Include test description, vendor alias, and indication with PA/claims
PA/panel-review actions are indicated per code in the table (eC PA, Review in panels, Not Covered); providers should include documentation (test description, vendor/test alias, clinical indication, and relevant diagnosis codes) to support PA or billing.
- Include the vendor/test alias as shown in the code table when available
- Document the clinical indication and matching diagnosis codes
Attach explanatory notes for unlisted codes (81479, 81599, 84999)
For unlisted molecular pathology (81479) and other unlisted codes (81599, 84999) include explanatory notes identifying the specific test and details sufficient for review when submitting the claim or PA request.
- Attach explanatory notes identifying the specific assay and vendor/lab
- Provide clinical rationale and documentation of medical necessity
Include test description and laboratory alias with requests
Each code entry includes a brief description and example vendor/test alias; include the test description and alias/laboratory when requesting prior authorization or submitting claims to support medical necessity.
Document diagnosis codes for diagnosis‑restricted tests
Some tests are covered only for specific diagnoses (for example, 0471U is covered for colorectal cancer diagnoses C18.0–C18.5); document the listed diagnosis code(s) on the PA request and claim.
- For 0471U include diagnosis C18.0–C18.5 as applicable
Denial risk for missing Evicore PA or panel review
Failure to obtain required Evicore prior authorization or to complete required panel review for codes marked 'eC PA' or 'Review in panels' may result in claim denial.
Initiate Evicore PA using the panel code that requires PA
If any procedure code in a multi‑test panel requires prior authorization, that procedure code should initiate the Evicore PA workflow; failure to submit the required PA for the triggering code may lead to denial of the panel.
Not‑covered tests will be denied if billed
Tests labeled 'Not Covered' for the member's line of business (Commercial, Medicaid, Priority Medicare) will be denied if billed for that plan; confirm plan‑level coverage status before ordering.
- Examples: multiple U‑codes and CPT entries are explicitly marked Not Covered in the tables
Panel‑level review may be required for 'Review in panels' codes
Some single‑gene tests and other entries are annotated 'Review in panels' — these require panel‑level review prior to coverage decisions; if included in a multi‑test panel, panel rules apply and PA must be initiated as noted.
Billing Not Covered tests risks denial and patient liability
Tests explicitly labeled 'Not Covered' in the tables will trigger claim denials when billed for the specified plan(s); review the Not Covered entries before ordering and consider alternative testing or patient financial responsibility discussions.
Not Covered entries and benefit‑rider exceptions may trigger denials
Tests marked 'Not Covered' or otherwise unsupported for the member's plan (e.g., codes listed as Not Covered for Medicaid or Priority Medicare) are denial triggers; verify plan status and benefit riders (e.g., Fertility Rider) before ordering.
Failure to obtain eC PA may cause denial
Many tests labeled 'eC PA' require electronic clinical prior authorization; failure to obtain Evicore authorization prior to service may result in denial for Commercial, Medicaid, and Priority Medicare plan members.
Not Covered — Exclusions and Explicit Non-Coverage
Prenatal cfDNA screening for sex chromosome aneuploidy, microdeletions, and single‑gene mutation screening are explicitly called out as investigational or not separately payable. The policy makes cfDNA testing for trisomies 21, 13, and 18 medically necessary under counseling and lab‑validated gestational age criteria, but states that cfDNA screening for sex chromosomes, less common trisomies, microdeletions, and single‑gene prenatal mutation screening are not covered or investigational/experimental.
The policy provides numerous examples of U‑codes and other proprietary codes designated Not Covered for certain payer lines; examples in the early U‑code window include 0008U, 0009U, 0010U, 0016U, 0017U and other U‑codes that are labeled Not Covered for Commercial, Medicaid, and Priority Medicare in the coding tables.
Additional examples of tests explicitly listed as Not Covered in specific code windows include U‑codes such as 0078U (pain management genotyping panel), 0086U (Accelerate PhenoTest BC kit), 0112U/0115U (selected infectious or respiratory panels), and other U‑codes and CPT entries shown as Not Covered for one or more plan types in the coding tables.
Many single‑gene blood group genotyping procedures and multiple Variantyx‑branded single‑gene or small‑panel analyses are listed with Not Covered status for Commercial and Medicaid plans (examples include 0180U–0183U and a range of 0212U–0238U entries). Providers should confirm the code‑level coverage stance before ordering blood group or related single‑gene tests.
The multianalyte risk score test 81506 (PreDx Diabetes Risk Score) is explicitly listed as Not Covered for Commercial, Medicaid, and Priority Medicare in the coding table.
Several additional tests across the U‑code windows and traditional CPT ranges are explicitly marked Not Covered. Examples in the document include lab and cytology codes such as 86352 (cellular function assays) and 88130 (sex chromatin/Barr body identification), both shown with Not Covered status in the coding tables.
The policy lists many specific U‑codes (for example 0078U, 0086U, 0112U, 0115U, 0152U, 0177U) and multiple red cell antigen genotyping codes as Not Covered for the designated plan types. These entries serve as explicit examples of codes that will not be reimbursed when billed under plans that list them as Not Covered.
Examples of U‑codes explicitly labeled Not Covered include 0238U, 0248U, 0249U, 0295U, 0301U, and 0302U — each of which is shown with a Not Covered payer disposition for one or more lines of business in the tables.
The coding listings include additional Not Covered examples such as 0310U (Kawasaki biomarker panel), 0323U (metagenomic NGS for CNS pathogens), and 0328U (large urine drug assay); these are explicitly marked Not Covered for the indicated plan types in the policy tables.
Specific PLA/HCPCS entries are flagged as Not Covered for one or more plan types — for instance, 0407U and 0429U are listed as Not Covered in the coding tables. Providers should reference the table to determine whether a given PLA code is payable for the member's plan.
A group of tests (for example 0490U, 0491U, 0492U, 0511U, 0512U, 0513U, 0532U, 0502U, 0500U) are explicitly shown as Not Covered across Commercial, Medicaid, and Priority Medicare in the document; these entries are examples of codes that will be denied if billed under the listed plan types.
The policy lists reproductive and embryo testing codes (such as PGT‑SR/PGT‑A entries 0555U, 0553U, 0554U and related PLA codes) with coverage notes; some reproductive testing codes are Not Covered unless a Fertility Rider is present. The table provides explicit per‑code descriptions and coverage dispositions that should be used to determine medical necessity and billing appropriateness.
Individual tests and CPT codes are designated Not Covered or OOS in the coding listings. For example, 0614U is Not Covered for Medicaid and Priority Medicare, and multiple traditional CPT lab codes are shown as OOS or Not Covered. Check the code table for plan‑specific dispositions before billing.
Definitions and Background
Genetic counseling interprets family and medical history, educates about inheritance patterns and testing options, and addresses psychosocial and ethical considerations. Counseling is required both before and after testing; for certain tests the policy requires counseling be performed by a board‑certified genetic counselor independent of the testing laboratory and that informed consent be documented in accordance with state law.
Coding — Key Values & Constraints
Revision History
Policy effective date set to 2026-06-01.
Committee review and last updated on 2026-05-13.
Next review scheduled on 2026-05-13.
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