GENETICS: COUNSELING, TESTING, SCREENING
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Defines Priority Health coverage criteria for genetic counseling, testing, and screening services, including medical necessity, prior authorization via Evicore for select tests, and management of specific tests; applies to Priority Health members and their providers.
New Policy Scope section added.
New FDA/Regulatory section added.
New Medical/Professional Society Guidelines section added.
New Government Regulations section listing applicable CMS NCDs or LCDs.
Coverage Criteria & Clinical Indications
General medical necessity
Covered when ALL of the following are met:
See Appendix A for conditions requiring counselor-delivered counseling; access Evicore via Priority Health Prism for authorization criteria.
Rapid Whole Genome Sequencing
Rapid whole genome sequencing (rWGS) is medically necessary when ALL of the following are met:
Priority Health requires notification of intent to perform inpatient rWGS via the Genetics medical policy prior notification form to avoid delays.
Prenatal cfDNA screening (NIPT)
Covered when ALL of the following are met:
Cell-free DNA screening for sex chromosomes and less common trisomies are not separately payable; cfDNA screening for microdeletions and single-gene prenatal cfDNA screening is considered investigational.
Exclusions / Not medically necessary
The following are exclusions and considered not medically necessary unless otherwise authorized by individual case review:
List is not all-inclusive; individual case review may allow coverage for investigational yet promising care with prior plan approval.
Testing of non-member relatives
Testing of non-member relatives may be covered when ALL of the following are met:
Testing that does not provide direct medical benefit to the member is not medically necessary unless criteria above are satisfied.
Per-code coverage actions (eC PA / Review in panels / Not Covered)
Per-code annotations in the coding lists indicate the payer action to apply for each listed code:
See individual code entries in the Coding section for the specific annotation per code and per plan.
Per-code coverage categorizations
Coverage stance is assigned per code in the coding lists; apply the corresponding process below:
Providers must submit required documentation and follow Evicore/Prism authorization steps.
Examples of Not Covered codes are listed in the Coding module (see per-code entries).
Verify per-code payer column before ordering.
Not Covered
The following tests and test categories are identified in the coding lists as Not Covered for the indicated plans:
Refer to the Coding module for the exact per‑code Not Covered designations by plan.
Prior Authorization Required (eC PA)
Tests labeled 'eC PA' require electronic prior authorization before testing may be billed for coverage:
Providers must submit clinical rationale and supporting documentation per Evicore criteria; failure to obtain PA may result in denial.
Priority Medicare — No PA required (OOS)
For Priority Medicare-designated codes:
Examples include select Genomic Unity single‑gene tests annotated OOS for Priority Medicare in the coding lists.
Coverage designations (per-code)
Coverage designations are provided per U-code and per plan; apply the listed designation when ordering/billing:
See individual U-code entries for aliases and specific lab/test names.
Confirm per-code plan column in the Coding section.
Review per-code entry for exact diagnosis list requirements.
Per-test coverage designations
Per-test coverage varies by code and by plan; examples below summarize common stances:
Refer to the Coding section for full per‑code plan mapping.
Providers must follow Evicore/Prism authorization pathways and submit required documentation.
General Coverage Stance
General coverage and prior authorization stance for listed procedures:
Examples: chromosome analysis and FISH codes (88264, 88267, 88269, 88271–88273) are OOS for eC - No PA; unlisted codes (81479, 81599, 88399, 89240) require explanatory notes with claims.
Exceptions and Prior Authorization
Exceptions and cases requiring specific benefit riders or prior authorization:
Claims for these codes require verification of fertility rider coverage.
Failure to obtain PA where indicated may result in denial.
Genetic counseling and testing are covered only when they meet medical necessity criteria and documentation requirements. Routine, ongoing, or long‑term genetic counseling and testing performed solely for paternity determination or to determine fetal sex are excluded. Prenatal cell‑free DNA screening limited to common fetal aneuploidies (trisomy 21, 13, 18) is covered when pre‑test education and counseling occur and the pregnancy and gestational age meet lab validation; by contrast, prenatal cfDNA screening for chromosome microdeletions and for single‑gene mutations is investigational and not payable. Testing of non‑member relatives may be considered only when the non‑member’s insurer has been billed and denied, testing provides direct medical benefit to the member, testing is the most cost‑effective option, testing is limited to up to five non‑member relatives in a member’s lifetime, and testing is recommended by a genetics counselor and approved by Priority Health. All genetic testing must be processed per the policy (Priority Health provider phlebotomist and laboratory) unless otherwise specified.
Certain emerging or menu‑based assays are explicitly considered investigational or not medically necessary. Chemosensitivity assays (live tumor cell culture drug‑response testing) are categorized as experimental/investigational and are not medically necessary. Prenatal cfDNA uses beyond standard aneuploidy screening (for example, microdeletions or single‑gene prenatal cfDNA) are also considered investigational. Providers seeking coverage for investigational testing may request individual case review, but such requests require prior plan approval and review by a Priority Health medical director or clinical pharmacist.
Covered Indications & Use Cases
CPT/PLA/U-code Listings & Code Tables
| 96041 | Medical genetics and genetic counseling services, each 30 minutes of total time provided by the genetic counselor on the date of the encounter |
| S0265 | Genetic counseling, under physician supervision, each 15 minutes |
| 81105 | Human Platelet Antigen 1 genotyping (HPA-1), ITGB3, gene analysis, common variant, HPA-1a/b |
| 81106 | Human Platelet Antigen 2 genotyping (HPA-2), GP1BA, gene analysis, common variant, HPA-2a/b |
| 81107 | Human Platelet Antigen 3 genotyping (HPA-3), ITGA2B, gene analysis, common variant, HPA-3a/b |
| 81105 | Human Platelet Antigen 1 genotyping (HPA-1) |
| 81106 | Human Platelet Antigen 2 genotyping (HPA-2) |
| 81107 | Human Platelet Antigen 3 genotyping (HPA-3) |
| 81108 | Human Platelet Antigen 4 genotyping (HPA-4) |
| 81109 | Human Platelet Antigen 5 genotyping (HPA-5) |
| 81110 | Human Platelet Antigen 6 genotyping (HPA-6w) |
| 81111 | Human Platelet Antigen 9 genotyping (HPA-9w) |
| 81112 | Human Platelet Antigen 15 genotyping (HPA-15) |
| 81120 | IDH1 common variants |
| 81121 | IDH2 common variants |
| 81225 | CYP2C19 gene analysis, common variants (eg, *2, *3, *4, *8, *17) |
| 81226 | CYP2D6 gene analysis, common variants (eg, *2, *3, *4, *5, *6, *9, *10, *17, *19, *29, *35, *41, *1XN, *2XN, *4XN) |
| 81227 | CYP2C9 gene analysis, common variants (eg, *2, *3, *5, *6) |
| 81228 | Cytogenomic (genome-wide) analysis for constitutional chromosomal abnormalities; CGH microarray analysis |
| 81229 | Cytogenomic analysis for copy number and SNP variants; CGH microarray analysis |
| 81230 | CYP3A4 gene analysis, common variant(s) (eg, *2, *22) |
| 81231 | CYP3A5 gene analysis, common variants (eg, *2, *3, *4, *5, *6, *7) |
| 81232 | DPYD gene analysis, common variant(s) (eg, *2A, *4, *5, *6) |
| 81233 | BTK gene analysis, common variants (eg, C481S, C481R) |
| 81234 | DMPK gene analysis; evaluation to detect expanded alleles (myotonic dystrophy type 1) |
| 81235 | EGFR gene analysis, common variants (eg, exon 19 LREA deletion, L858R, T790M, G719A/S, L861Q) |
| 81236 | EZH2 gene analysis, full gene sequence |
| 81237 | EZH2 gene analysis, common variant(s) (eg, codon 646) |
| 81238 | F9 full gene sequence (hemophilia B) |
| 81239 | DMPK characterization of alleles (expanded size) |
| 81240 | F2 prothrombin 20210G>A variant analysis |
| 81241 | F5 Factor V Leiden variant analysis |
| 81242 | FANCC gene analysis, common variant (eg, IVS4+4A>T) |
| 81243 | FMR1 evaluation to detect expanded alleles (Fragile X) |
| 81244 | FMR1 characterization of alleles (expanded size and promoter methylation) |
| 81245 | FLT3 internal tandem duplication (ITD) variants analysis (exons 14,15) |
| 81246 | FLT3 tyrosine kinase domain (TKD) variants analysis (eg, D835, I836) |
| 81247 | G6PD gene analysis; common variant(s) (eg, A, A-) |
| 81248 | G6PD known familial variant(s) |
| 81249 | G6PD full gene sequence |
| 81250 | G6PC gene analysis, common variants (eg, R83C, Q347X) |
| 81251 | GBA gene analysis, common variants (eg, N370S, 84GG, L444P) |
| 81252 | GJB2 full gene sequence (nonsyndromic hearing loss) |
| 81253 | GJB2 known familial variants |
| 81254 | GJB6 common deletion variants (eg, del(GJB6-D13S1830), del(GJB6-D13S1854)) |
| 81255 | HEXA gene analysis, common variants (eg, 1278insTATC, 1421+1G>C, G269S) |
| 81256 | HFE gene analysis, common variants (eg, C282Y, H63D) |
| 81257 | HBA1/HBA2 gene analysis for common deletions/variants (alpha thalassemia) |
| 81258 | HBA1/HBA2 known familial variant |
| 81259 | HBA1/HBA2 full gene sequence |
| 81260 | IKBKAP gene analysis, common variants (eg, 2507+6T>C, R696P) |
| 81261 | IGH@ gene rearrangement analysis; amplified methodology |
| 81262 | IGH@ gene rearrangement analysis; direct probe methodology |
| 81263 | IGH@ variable region somatic mutation analysis |
| 81264 | IGK@ gene rearrangement analysis |
| 81265 | Comparative STR analysis (patient and comparative specimen) |
| 81266 | Comparative STR analysis; each additional specimen |
| 81267 | Chimerism (engraftment) analysis, without cell selection |
| 81268 | Chimerism analysis, with cell selection, each cell type |
| 81269 | HBA1/HBA2 duplication/deletion variants |
| 81270 | JAK2 p.Val617Phe (V617F) variant analysis |
| 81271 | HTT evaluation to detect expanded alleles (Huntington disease) |
| 81291 | CODE ENTRY (listed in segment) |
| 81292 | MLH1 gene analysis; full sequence analysis |
| 81293 | MLH1 gene analysis; known familial variants |
| 81294 | MLH1 gene analysis; duplication/deletion variants |
| 81295 | MSH2 gene analysis; full sequence analysis |
| 81296 | MSH2 gene analysis; known familial variants |
| 81297 | MSH2 gene analysis; duplication/deletion variants |
| 81298 | MSH6 gene analysis; full sequence analysis |
| 81299 | MSH6 gene analysis; known familial variants |
| 81300 | MSH6 gene analysis; duplication/deletion variants |
| 81351 | TP53 full gene sequence |
| 81352 | TP53 targeted sequence analysis |
| 81353 | TP53 known familial variant |
| 81354 | Cytogenomic (genome-wide) analysis; OGM |
| 81355 | VKORC1 common variant(s) |
| 81357 | U2AF1 common variants |
| 81360 | ZRSR2 common variants |
| 81361 | HBB common variants (eg HbS, HbC) |
| 81362 | HBB known familial variant(s) |
| 81363 | HBB duplication/deletion variants |
| 81552 | Oncology (uveal melanoma), mRNA gene expression profiling of 15 genes; risk of metastasis. |
| 81554 | Pulmonary disease (IPF), mRNA gene expression of 190 genes; diagnostic algorithm (probability of UIP). |
| 81558 | Transplantation medicine (kidney allograft rejection), mRNA profiling of 139 genes from whole blood; binary outcome for transplant excellence or not. |
| 81595 | Cardiology (heart transplant), mRNA gene expression profiling of 20 genes; rejection risk score. Alias: AlloMap®. |
| 81596 | Infectious disease (chronic HCV), six biochemical assays; prognostic scores for fibrosis and necroinflammatory activity. Alias: Fibrotest/Fibrosure. |
| 81599 | Unlisted multianalyte assay with algorithmic analysis; explanatory notes identifying specific test must accompany claim. |
| 84999 | Unlisted chemistry procedure; explanatory notes identifying specific test must accompany claim. |
| 0002M | Liver disease, ten biochemical assays; prognostic algorithm (NASH FibroSURE) |
| 0003M | Liver disease, ten biochemical assays; prognostic algorithm (NASH FibroSURE) |
| 0004M | Scoliosis, DNA analysis of 53 SNPs; prognostic risk score (ScoliScore) |
| 0006M | Oncology (hepatic), mRNA expression of 161 genes with AFP; risk classifier (HeproDX) |
| 0007M | Oncology (GI NET), PCR expression analysis of 51 genes; tumor disease index (NETest) |
| 0011M | Oncology (prostate), mRNA assay of 12 genes in plasma/urine; predicts high-grade prostate cancer risk |
| 0012M | Oncology (urothelial), mRNA profiling of five genes in urine; risk score for urothelial carcinoma (CxBladder) |
| 0013M | Oncology (urothelial), mRNA profiling for recurrence (CxBladder Monitor) |
| 0016M | Oncology (bladder), mRNA microarray profiling of 219 genes; molecular subtype classification (Decipher Bladder) |
| 0017M | Oncology (DLBCL), mRNA expression profiling of 20 genes; cell of origin (Lymph2Cx) |
| 0005U | COMMERCIAL PLANS = Not Covered; MEDICAID = Not Covered; PRIORITY MEDICARE = Not Covered. |
| 0010U | COMMERCIAL PLANS = Not Covered; MEDICAID = Not Covered; PRIORITY MEDICARE = Not Covered. |
| 0040U | COMMERCIAL PLANS = Not Covered; MEDICAID = Not Covered; PRIORITY MEDICARE = Not Covered. |
| 0046U | COMMERCIAL PLANS = Not Covered; MEDICAID = Not Covered; PRIORITY MEDICARE = Not Covered. |
| 0049U | COMMERCIAL PLANS = Not Covered; MEDICAID = Not Covered; PRIORITY MEDICARE = Not Covered. |
| 0055U | COMMERCIAL PLANS = Not Covered; MEDICAID = Not Covered; PRIORITY MEDICARE = Not Covered. |
| 0073U | listed; coverage = eC PA (MEDICAID = eC PA, PRIORITY MEDICARE = eC PA) |
| 0074U | CYP2D6 targeted sequence analysis (non-duplicated gene when duplication/multiplication is trans); COMMERCIAL PLANS = eC PA; MEDICAID = eC PA; PRIORITY MEDICARE = eC PA |
| 0075U | CYP2D6 5' gene duplication/multiplication targeted sequence analysis; COMMERCIAL PLANS = eC PA; MEDICAID = eC PA; PRIORITY MEDICARE = eC PA |
| 0076U | CYP2D6 3' gene duplication/multiplication targeted sequence analysis; COMMERCIAL PLANS = eC PA; MEDICAID = eC PA; PRIORITY MEDICARE = eC PA |
| 0078U | Pain management genotyping panel, 16 variants; COMMERCIAL PLANS = Not Covered; MEDICAID = Not Covered; PRIORITY MEDICARE = Not Covered |
| 0084U | Red blood cell antigen typing, DNA, genotyping of 10 blood groups; COMMERCIAL PLANS = eC PA; MEDICAID = eC PA; PRIORITY MEDICARE = eC PA |
| 0086U | Infectious disease organism identification, blood culture rRNA FISH, 6+ targets; COMMERCIAL PLANS = Not Covered; MEDICAID = Not Covered; PRIORITY MEDICARE = Not Covered |
| 0087U | Cardiology (heart transplant) mRNA gene expression profiling of 1283 genes; COMMERCIAL PLANS = eC PA; MEDICAID = eC PA; PRIORITY MEDICARE = eC PA |
| 0088U | Kidney allograft rejection microarray profiling of 1494 genes; COMMERCIAL PLANS = eC PA; MEDICAID = eC PA; PRIORITY MEDICARE = eC PA |
| 0089U | Oncology (melanoma) gene expression profiling via adhesive patch; COMMERCIAL PLANS = OOS for eC - No PA required; MEDICAID = Not Covered; PRIORITY MEDICARE = OOS for eC - No PA required |
| 0181U | Navigator CO Sequencing / Grifols Immunohematology Center — COMMERCIAL PLANS = Not Covered; MEDICAID = Not Covered; PRIORITY MEDICARE = Not Covered |
| 0182U | Red cell antigen (Cromer) genotyping CD55 exons 1-10; Not Covered |
| 0183U | Red cell antigen (Diego) genotyping SLC4A1 exon 19; Not Covered |
| 0184U | Red cell antigen (Dombrock) genotyping ART4 exon 2; Not Covered |
| 0185U | Red cell antigen (H) genotyping FUT1 exon 4; Not Covered |
| 0186U | Red cell antigen (H) genotyping FUT2 exon 2; Not Covered |
| 0187U | Red cell antigen (Duffy) genotyping ACKR1 exons 1-2; Not Covered |
| 0189U | Red cell antigen (MNS) genotyping GYPA introns/exon 2; Not Covered |
| 0190U | Red cell antigen (MNS) genotyping GYPB introns/pseudoexon 3; Not Covered |
| 0191U | Red cell antigen (Indian) genotyping CD44 exons 2,3,6; Not Covered |
| 0203U | PredictSURE IBD Test (mRNA, IBD aggressiveness, 17 genes) — COMMERCIAL PLANS = eC PA |
| 0205U | Vita Risk (AMD test, 3 gene variants) — COMMERCIAL PLANS = eC PA |
| 0209U | CNGnome (melanoma mRNA profiling, 23 genes) — COMMERCIAL PLANS = eC PA |
| 0211U | MI Cancer Seek NGS Analysis (pan-tumor DNA/RNA NGS) — COMMERCIAL PLANS = eC PA |
| 0212U | Genomic Unity Exome Plus Analysis - Proband (whole genome & mitochondrial) — Not Covered |
| 0213U | Genomic Unity Whole Genome Analysis - Comparator — Not Covered |
| 0214U | Genomic Unity Exome Plus Analysis - Proband (alternate listing) — eC PA |
| 0215U | Genomic Unity Exome Plus Analysis - Comparator — eC PA |
| 0216U | Genomic Unity Ataxia Repeat Expansion and Sequence Analysis (12 genes) — eC PA |
| 0217U | Genomic Unity Comprehensive Ataxia Repeat Expansion and Sequence Analysis (51 genes) — eC PA |
| 0260U | Optical genome mapping for rare/constitutional/heritable disorders |
| 0262U | Oncology (solid tumor), gene expression profiling by RT‑PCR of 7 gene pathways |
| 0264U | Optical genome mapping for rare/constitutional/heritable disorders |
| 0265U | Whole genome and mitochondrial DNA sequence analysis for rare constitutional/heritable disorders |
| 0266U | Whole-transcriptome tissue-specific gene expression for unexplained constitutional/heritable disorders |
| 0267U | Optical genome mapping and whole genome sequencing for rare constitutional disorders |
| 0268U | Genomic sequence analysis of 15 genes for atypical hemolytic uremic syndrome (aHUS) |
| 0269U | Genomic sequence analysis of 14 genes for autosomal dominant congenital thrombocytopenia |
| 0270U | Genomic sequence analysis of 20 genes for congenital coagulation disorders |
| 0271U | Genomic sequence analysis of 23 genes for congenital neutropenia |
| 0328U | Alias/Test Name examples listed; COMMERCIAL PLANS = Not Covered; MEDICAID = Not Covered; PRIORITY MEDICARE = Not Covered |
| 0329U | Oncology exome and transcriptome sequence analysis with tumor and normal subtraction; COMMERCIAL PLANS = eC PA; MEDICAID = eC PA; PRIORITY MEDICARE = eC PA |
| 0330U | Infectious agent detection vaginal pathogen panel (27 organisms); COMMERCIAL PLANS = Not Covered; MEDICAID = Not Covered; PRIORITY MEDICARE = Not Covered |
| 0331U | Optical genome mapping for hematolymphoid neoplasia; COMMERCIAL PLANS = eC PA; MEDICAID = eC PA; PRIORITY MEDICARE = eC PA |
| 0332U | Epigenetic 8-marker qPCR predicting checkpoint-inhibitor response; COMMERCIAL PLANS = eC PA; MEDICAID = eC PA; PRIORITY MEDICARE = eC PA |
| 0333U | HCC surveillance cfDNA methylation + AFP/AFP-L3/DCP algorithm; COMMERCIAL PLANS = eC PA; MEDICAID = eC PA; PRIORITY MEDICARE = eC PA |
| 0334U | Targeted tumor sequencing (>=84 genes) FFPE; COMMERCIAL PLANS = eC PA; MEDICAID = eC PA; PRIORITY MEDICARE = eC PA |
| 0335U | Whole genome sequence analysis for rare/heritable disorders (proband); COMMERCIAL PLANS = eC PA; MEDICAID = eC PA; PRIORITY MEDICARE = eC PA |
| 0336U | Whole genome sequence analysis comparator (eg parent); COMMERCIAL PLANS = eC PA; MEDICAID = eC PA; PRIORITY MEDICARE = eC PA |
| 0339U | Prostate mRNA HOXC6/DLX1 expression test (SelectMDx); COMMERCIAL PLANS = eC PA; MEDICAID = eC PA; PRIORITY MEDICARE = eC PA |
| 0433U | Oncology (prostate), 5 DNA regulatory markers by qPCR, whole blood (EpiSwitch® Prostate Screening Test) |
| 0434U | Drug metabolism genomic panel, 25 genes (RightMed® Gene Test) |
| 0437U | Psychiatry (anxiety), mRNA expression profiling of 15 biomarkers, whole blood |
| 0438U | Drug metabolism buccal specimen panel, 33 genes including CYP2D6 del/dup |
| 0439U | Cardiology (CHD), DNA SNPs and methylation markers qPCR/digital PCR, algorithmic risk |
| 0444U | Oncology (solid organ), targeted genomic sequencing panel of 361 genes from FFPE |
| 0449U | Carrier screening panel including CFTR, SMN1, HBB, HBA1, HBA2 |
| 0452U | Oncology (bladder), methylated PENK DNA detection by LTE-aMSP, urine |
| 0453U | Oncology (colorectal cancer), cfDNA methylation-based qPCR assay (SEPTIN9, IKZF1, BCAT1, others) |
| 0454U | Rare disease optical genome mapping for CNVs, inversions, translocations |
| 0460U | Oncology, DNA SNP genotyping by real-time PCR of 24 genes, reported phenotypes (RightMed® Oncology Gene Report) |
| 0461U | Oncology pharmacogenomic analysis of 24 genes by real-time PCR |
| 0463U | Oncology (cervix), mRNA profiling of 14 biomarkers (Proofer '7 HPV mRNA E6/E7) — Not Covered |
| 0471U | Oncology (colorectal cancer), qualitative real-time PCR of 35 KRAS/NRAS variants; coverage limited to specified ICD-10 diagnoses |
| 0473U | Oncology (solid tumor), NGS of FFPE tissue with matched normal, 648 genes |
| 0474U | Hereditary pan-cancer germline panel, 88 genes |
| 0475U | Hereditary prostate cancer panel, 23 genes plus del/dup when indicated |
| 0476U | Drug metabolism psychiatry, genotyping of 14 genes plus CYP2D6 CNV (RightMed® MentalHealth) |
| 0477U | Drug metabolism psychiatry, 14 genes plus CYP2D6 CNV with gene-drug interactions |
| 0478U | Oncology (NSCLC), DNA/RNA digital PCR analysis of 9 genes for actionable variants |
| 0481U | IDH1, IDH2, and TERT promoter mutation analysis by NGS (CNS tumors) |
| 0485U | Oncology (solid tumor), cfDNA and RNA NGS with interpretive report for germline, CHIP, and tumor-derived variants (Caris Assure) |
| 0486U | Oncology (pan-solid tumor), NGS methylation analysis of cfDNA (Northstar Response) |
| 0487U | Oncology (solid tumor), cfDNA targeted NGS panel of 84 genes (Northstar Select) |
| 0488U | Obstetrics NIPT for fetal antigen(s) (Rh, Kell, Duffy) using cfDNA (UNITY Fetal Antigen) |
| 0489U | Obstetrics single-gene NIPT for paternal variants and maternal mutation dosage (UNITY Fetal Risk) |
| 0490U | Oncology (melanoma), circulating melanoma cell enumeration (CELLSEARCH® CMC) — Not Covered |
| 0491U | Oncology (solid tumor), circulating tumor cell enumeration with ER quantification (CELLSEARCH® ER) — Not Covered |
| 0492U | Oncology (solid tumor), circulating tumor cell enumeration with PD-L1 quantification (CELLSEARCH® PDL1) — Not Covered |
| 0493U | Transplantation medicine, donor-derived cfDNA quantification (Prospera™) |
| 0491U | CELLSEARCH® PDL1 Circulating Tumor Cell Test (EpCAM, cytokeratins, CD45, PD-L1), peripheral blood |
| 0492U | CELLSEARCH® PDL1 Circulating Tumor Cell Test (alias listed) |
| 0493U | Donor-derived cell-free DNA quantification (Prospera™) |
| 0494U | Fetal RhD gene analysis from maternal cfDNA (Rh Test, Natera) |
| 0495U | Prostate panel (plasma proteins + polygenic risk score) (Stockholm3) |
| 0496U | Colorectal ctDNA: mutations, methylation, proteins (ColoScape™ PLUS) |
| 0497U | Prostate mRNA expression profiling (OncoAssure™ Prostate) |
| 0498U | Colorectal NGS and methylation panel (OptiSeq™ Colorectal Cancer NGS Panel) |
| 0499U | Colorectal and lung 8-gene NGS panel (OptiSeq™ Dual Cancer Panel Kit) |
| 0500U | UBA1 targeted variant analysis for VEXAS syndrome (QClamp® Plex VEXAS) |
| 82172 | Apolipoprotein, each — OOS for eC - No PA required |
| 83006 | Growth stimulation expressed gene 2 (ST2) — OOS for eC - Not Covered |
| 83950 | Oncoprotein; HER-2/neu — OOS for eC - No PA required |
| 83951 | Oncoprotein; des-gamma-carboxy-prothrombin (DCP) — OOS for eC - Not Covered |
| 83993 | Calprotectin, fecal — OOS for eC- No PA required |
| 84233 | Receptor assay; estrogen — OOS for eC- No PA required |
| 84234 | Receptor assay; progesterone — OOS for eC- No PA required |
| 86152 | Cell enumeration (eg circulating tumor cells) — OOS for eC - Not Covered |
| 86153 | Cell enumeration w/ physician interpretation — OOS for eC - Not Covered |
| 86294 | Immunoassay for tumor antigen, qualitative (eg, BTA Stat) — OOS for eC- No PA required; covered only for specified bladder diagnoses |
| 88264 | Chromosome analysis (mentioned as required). |
| 88267 | Chromosome analysis, amniotic fluid or chorionic villus, count 15 cells, 1 karyotype, with banding. |
| 88269 | Chromosome analysis, in situ for amniotic fluid cells, count cells from 6-12 colonies, 1 karyotype, with banding. |
| 88271 | Molecular cytogenetics; DNA probe, each (eg, FISH). |
| 88272 | Molecular cytogenetics; chromosomal in situ hybridization, analyze 3-5 cells (eg, for derivatives and markers). |
| 88273 | Molecular cytogenetics; chromosomal in situ hybridization, analyze 10-30 cells (eg, for microdeletions). |
| 88274 | Molecular cytogenetics; interphase in situ hybridization, analyze 25-99 cells. |
| 88275 | Molecular cytogenetics; interphase in situ hybridization, analyze 100-300 cells. |
| 88280 | Chromosome analysis; additional karyotypes, each study. |
| 88283 | Chromosome analysis; additional specialized banding technique (eg, NOR, C-banding). |
Provider Actions, Prior Authorization & Documentation
Obtain Evicore prior authorization for selected tests
Prior authorization for selected genetic tests and many procedure codes must be obtained through Evicore via Priority Health Prism; the policy states selected tests require prior authorization administered through Evicore and directs providers to Log into Priority Health Prism → Authorizations → Authorization Criteria Lookup to access Evicore guidelines.
- Applies notably to procedure codes in the 81105–81599 range and many listed CPT/PLA codes.
- Initiate the Evicore request using the procedure code that requires PA via the provider portal.
Submit eC PA for specified hereditary and key gene tests
Many hereditary and clinically significant gene tests are designated 'eC PA' and require electronic prior authorization for Commercial, Medicaid, and Priority Medicare lines; providers must submit PA per the payer's electronic workflow.
- Examples include BRCA1/BRCA2 (81162–81165) and multiple pharmacogenomic genes (81225–81227).
- Follow the eC PA process shown in per-code entries when billing.
Expect panel-level review for 'Review in panels' codes
Some codes are designated 'Review in panels'—these codes are reviewed as part of a panel; they may be covered without PA when reported alone but will be subject to panel review or PA if reported with codes that require authorization.
- Examples: multiple HLA, tumor, and single-gene entries noted as 'Review in panels'.
- If included in a multi-code panel where any code requires PA, the procedure code that requires PA should trigger Evicore access.
Follow annotated PA or panel review processes
Where a code is annotated as 'eC PA' or 'Review in panels' the provider must follow the payer's electronic clinical prior authorization or panel review process before testing or billing.
- Use the procedure code requiring PA to initiate Evicore via the provider portal.
- If codes are reported together, obtain PA for the code that requires authorization to avoid panel combination denial risk.
Obtain electronic prior authorization for eC PA codes
Numerous CPT codes in the molecular/genetics sections are marked 'eC PA'—electronic prior authorization is required for coverage determination and must be obtained prior to testing.
Anticipate panel review for listed CPT codes
Several CPT codes are marked 'Review in panels'; coverage decisions for these codes are made within panel-level review rather than as individually pre-approved tests—providers should expect clinical review and supply requested documentation.
Obtain electronic clinical prior authorization for eC PA codes
Codes annotated 'eC PA' require electronic clinical prior authorization for Commercial, Medicaid, and Priority Medicare plans; obtain the eC PA before testing to avoid coverage delays or denials.
No PA required for 81420 (NIPT), but document counseling and indications
Code 81420 (fetal chromosomal aneuploidy cfDNA panel for chromosomes 13, 18, 21) is designated 'No PA required'; however, documentation must still support medical necessity and pre-test counseling per policy.
- Provide documentation of appropriate education and counseling prior to testing.
- Ensure gestational age and pregnancy type (singleton/twin) meet laboratory-validated criteria.
Obtain eC PA for many listed CPT/PLA codes
Many CPT and PLA U-codes in the lists are annotated 'eC PA' indicating electronic case review/prior authorization is required for Commercial, Medicaid, and Priority Medicare plans; obtain prior authorization through the eC process for those codes.
Verify per-code 'No PA Required' exceptions before ordering
Certain tests are explicitly listed as 'No PA Required' (OOS or No PA) — examples include some fetal aneuploidy cfDNA entries and screening tests such as Cologuard; verify per-code payer columns before ordering.
Obtain eC PA for listed proprietary and panel tests
The per-code listings identify many tests that require electronic prior authorization ('eC PA'); when a test is listed as eC PA providers must obtain authorization through the electronic claims/prior authorization process before testing or billing.
- Examples span proprietary U-codes and multi-gene panels where eC PA is the listed coverage action.
- Follow Evicore via Priority Health Prism for submission and required documentation.
0003U is OOS for commercial plans (no PA) — verify payer column for coverage
Code 0003U (Overa/OVA1 Next Generation) is listed as OOS for commercial plans and requires no PA for in-network providers; Medicaid is listed as Not Covered for this test.
- Confirm plan-specific status before ordering; OOS indicates out-of-scope for Evicore management and No PA required for in-network providers.
- If member has Medicaid, the code is Not Covered per the listing.
Check per-code coverage/PA notes (No PA required vs Not Covered)
Per-code payer columns show some codes explicitly labeled 'No PA required' or 'Not Covered' depending on the plan; providers must verify the code-specific payer column (Commercial/Medicaid/Priority Medicare) prior to ordering and billing.
Obtain eC PA via electronic claims/prior authorization for eC PA codes
Codes listed as 'eC PA' require prior authorization through the payer's electronic prior authorization process; obtain the eC PA before performing or billing the test to meet coverage requirements.
- This applies to many U-code proprietary tests and newer PLA entries designated eC PA.
- Submit required clinical rationale and supporting documentation in the eC PA request.
eC PA required before billing for 'eC PA' tests
Tests identified as 'eC PA' in code entries must have electronic prior authorization per the plan designation; providers should not proceed without completing the eC PA workflow for those codes.
- This is reiterated across many code groups—eC PA is the expected authorization pathway for panels, cfDNA, and specialty tests.
- Follow Evicore/Prism instructions to submit complete clinical information.
Obtain PA for many proprietary molecular/genetic tests
Numerous proprietary molecular/genetic tests (U-codes and PLA codes) are designated 'eC PA' across Commercial, Medicaid, and Priority Medicare — obtain prior authorization per the payer policy for these tests before testing.
Obtain eC PA for U-code proprietary tests before billing
Many U-codes in the U-code listings are labeled 'eC PA' indicating electronic claim prior authorization is required for coverage; obtain prior authorization through Evicore/Priority Health Prism when billing these U-codes.
Obtain evidence-based clinical prior authorization for many tests
Many listed tests across sections are labeled 'eC PA' for Commercial, Medicaid, and Priority Medicare; providers must obtain evidence-based clinical prior authorization per the payer policy before testing.
Secure eC PA for PLA/U-code tests per plan annotations
Tests marked 'eC PA' in the PLA/test code listings require electronic clinical prior authorization before they will be covered for the specified plan(s); secure the eC PA via the payer's system.
- Examples include many PLA codes in the 0490–0578U range and beyond.
- Include diagnosis, prior testing, specimen type, and test description in the PA submission as indicated.
Obtain eC PA for listed U-codes via Evicore
Multiple U-codes in the later U-code lists are designated 'eC PA' for commercial, Medicaid, and Priority Medicare; providers must obtain electronic prior authorization for these U-codes prior to testing or billing.
Follow Priority Health/ Evicore PA and benefit-rider rules
Certain genetic tests require prior authorization via Priority Health systems or are covered only with specific benefit riders; providers should follow Evicore guidelines via Priority Health Prism and submit requests demonstrating medical necessity.
Document genetic counseling and informed consent
Document that pre- and post-test genetic counseling occurred and retain informed consent records; Michigan law (Public Health Code Act 368 of 1978: 333.17020) requires informed consent for genetic testing.
- Genetic counseling must be by a board‑certified genetic counselor independent of the testing laboratory for specified conditions.
- Document counseling and informed consent in the medical record prior to testing.
Initiate PA using the procedure code that requires authorization
Initiate Evicore prior authorization using the procedure code that requires PA; the policy specifies the procedure requiring PA should initiate access to Evicore via the provider portal.
- If multiple codes are reported, use the procedure code that requires PA to start the Evicore request.
- Access Evicore via Priority Health Prism → Authorizations → Authorization Criteria Lookup.
Follow eC PA and panel review workflows
When a code is annotated 'eC PA' or 'Review in panels' providers must follow the payer's eC PA or panel review process and supply requested clinical evidence during the electronic review.
- Follow Evicore guidance for clinical documentation and criteria submission via Priority Health Prism.
- Panel-reviewed codes may require additional clinical justification beyond single-code claims.
Include concise test description (genes/type of analysis) on PA/claim
Provide a brief test description with claims or prior authorization requests (including gene names and type of analysis) as many CPT entries include a test description and the policy expects this supporting information.
- Include gene names, panel size, and type of analysis (DNA/RNA/mitochondrial/cfDNA) in the PA or claim documentation.
- For unlisted codes, include explanatory notes identifying the specific test.
Document NIPT clinical rationale despite No PA for 81420
Even when 81420 is designated 'No PA required', providers should still document counseling and the clinical indication to support medical necessity per the policy's prenatal testing section.
- Document pre-test education and counseling, pregnancy type, and laboratory-validated gestational age.
- Provide supporting documentation with the claim when requested.
Attach explanatory notes when billing unlisted codes
When billing unlisted codes (e.g., 81479, 81599, 84999) include explanatory notes identifying the specific test and the methodology; the policy requires explanatory notes to accompany claims for unlisted procedures.
- Attach explanatory notes that identify the test name, method, genes/panels interrogated, and clinical rationale.
- Failure to include explanatory notes may impede adjudication or result in denial.
Provide explanatory notes with unlisted-code claims
Unlisted codes such as 81599 and 84999 must be accompanied by explanatory documentation identifying the specific test when submitting claims.
- Provide test name, lab alias, methodology, and clinical justification with the claim.
- Use explanatory notes to clarify the billed service for adjudication.
Obtain PA for tests annotated 'eC PA'
Providers must obtain prior authorization where tests are listed as 'eC PA'—the policy repeatedly instructs that tests marked eC PA require electronic prior authorization per the plan designations.
- This operational requirement applies across CPT, PLA, and U-code entries annotated 'eC PA'.
- Submit requisite clinical documentation and test details via Evicore/Priority Health Prism.
Use eC PA process for tests labeled 'eC PA'
Tests designated 'eC PA' require electronic prior authorization; providers should use the electronic PA process to secure authorization prior to testing and claims submission.
- This is an operational reminder repeated throughout the per-code listings.
- Include diagnosis, prior testing, specimen type, and brief test description in the eC PA request.
Obtain eC PA before claims submission for eC PA tests
When a test is labeled 'eC PA' the provider must obtain prior authorization through the electronic clinical prior authorization process before submitting a claim; failure to do so may result in denial.
- Examples: multiple U-codes and PLA codes list eC PA—obtain PA via Evicore prior to performing the test.
- Provide complete clinical justification and attach supporting reports as requested.
Submit specimen source and report documentation with PA/claims
Include specimen source and the laboratory report showing clinically significant findings when submitting documentation; many code descriptions specify specimen requirements (eg, plasma for cfDNA, tumor and normal blood/saliva for paired tumor-normal testing).
- Examples: Signatera (0340U) requires prior tumor/germline NGS context; cfDNA assays request plasma specimen documentation.
- Attach lab reports and specimen source documentation with PA requests and claims.
Include required ICD‑10 when test coverage is diagnosis‑limited
Provide the correct ICD‑10 diagnosis codes when coverage is diagnosis‑specific; certain tests (eg, 0471U CRCdx RAS kit) are covered only for listed ICD‑10 codes and claims should include the indicated diagnosis.
- 0471U is covered only for colorectal cancer ICD‑10 codes C18.0–C18.9, C19, C20, C21.0–C21.8.
- Verify and include the covered diagnosis code on the PA request and claim.
Failure to obtain required eC PA may lead to denial
Many tests labeled 'eC PA' require prior authorization; failure to obtain required PA through Evicore or the eC process may lead to denial or medical necessity review.
- Obtain eC PA for codes annotated 'eC PA' before testing or billing.
- If testing is urgent, notify Priority Health/Evicore per Evicore guidelines to avoid delays.
Include specified diagnosis codes for diagnosis‑restricted tests
When coverage for a test is limited to specific diagnoses (example: 86294 BTA Stat for specified bladder diagnoses), include the appropriate diagnosis code to support coverage.
- 86294 is covered only for diagnoses C67.0–C67.9, D09.0, D49.4, and Z85.51.
- Claims without the required diagnosis may be denied or returned for clarification.
Attach explanatory notes for unlisted codes with claims
Unlisted procedure codes (e.g., 81599, 84999, 88299, 89240, 88399) require explanatory notes identifying the specific test or procedure when billed; attach detailed explanatory documentation to the claim.
- Explain the test methodology, genes/panels interrogated, clinical indication and lab performing the test.
- Failure to include explanatory notes may delay processing or trigger denial.
Denial risk if Evicore PA not obtained where required
Failure to obtain prior authorization via Evicore for selected tests may result in claim denial or requirement for retrospective review; obtain PA before testing when codes are annotated as requiring Evicore authorization.
- Evicore-managed tests include many codes in the 81105–81599 range and numerous U-codes; access Evicore via Priority Health Prism.
- Denials are likely if required prior authorization is not obtained.
Not Covered procedures: no PA required but voluntary authorization possible
Procedures that are explicitly 'Not Covered' do not require prior authorization, but providers may submit voluntary authorization requests for a non‑coverage determination if desired; verify per-code coverage status before ordering.
- Not Covered entries (per payer column) will be denied if billed under that plan.
- Voluntary authorization can be requested for non‑coverage determination in selected cases.
Panel combination denial risk — obtain PA for the code that requires it
When multiple procedure codes within the 81105–81599 range are reported as part of a panel, all included procedure codes are subject to medical necessity review if any code requires prior authorization; obtain PA for the code that requires it to reduce panel combination denial risk.
- If a multi-code panel contains any eC PA code, the entire panel may be reviewed.
- Use the procedure code requiring PA to initiate the Evicore request to document the clinical rationale for the panel.
Not Covered codes will be denied if billed under the listed plan
Tests explicitly annotated 'Not Covered' in the per‑code listings will be denied if submitted for coverage under the listed plan(s); verify the Not Covered annotations in code columns prior to ordering.
- Examples: selected single-gene and PLA codes annotated Not Covered for certain plans (eg, 81324 PMP22 Not Covered for Medicaid and Priority Medicare).
- Do not expect reimbursement for codes marked Not Covered for the member's plan.
Per-code 'Not Covered' annotations indicate high denial risk
Some CPT and PLA codes are explicitly listed as 'Not Covered' for certain lines of business (Commercial, Medicaid, Priority Medicare); billing those codes for affected plans is likely to trigger denial—check the code-specific payer column.
- Examples include 81324 (PMP22 duplication/deletion) and several U-codes shown as Not Covered in the per-code listings.
- If a test is needed despite Not Covered status, consider submitting a voluntary non-coverage determination request as noted.
Lack of required eC PA may trigger denial
Tests labeled 'eC PA' in the policy require electronic clinical prior authorization; failure to obtain such authorization before testing or billing may result in denial.
- This operational requirement applies across CPT, PLA, and U-code entries designated eC PA.
- Obtain PA through Evicore/Priority Health Prism and include required clinical documentation.
Obtain eC case review to avoid denials for eC PA codes
Many tests require electronic case review (eC PA); failure to obtain electronic case review/prior authorization where indicated (most CPT entries list 'eC PA') may trigger claim denial.
- Obtain eC PA for codes annotated 'eC PA' to avoid denials.
- If uncertain, verify the code's per-plan annotation before testing.
Not Covered tests are denial triggers when billed
Tests explicitly labeled 'Not Covered' in the PLA/CPT/U-code entries (many listed examples) will be denied if submitted for coverage under the listed plan(s); providers should avoid billing those tests under those plans.
- Examples include many PLA U-codes and select CPT codes annotated as Not Covered across plan columns.
- Confirm member coverage and consider alternative testing or documentation if clinically necessary.
Billing 'Not Covered' tests to the listed plan will likely be denied
Tests listed as 'Not Covered' in the per-code entries will be denied if billed under the specified plan(s); providers should verify Not Covered status for the member's plan before ordering.
Routinely check Not Covered PLA code ranges to avoid denials
Multiple contiguous PLA/CPT codes and ranges are explicitly marked 'Not Covered' in the policy (examples shown) and will be denied if billed under the listed plans; providers must check each code's plan column before ordering.
- The 0181U–0200U range contains many red blood cell antigen genotyping tests marked Not Covered.
- Avoid billing Not Covered PLA codes to the affected plans.
Program‑specific 'Not Covered' status will trigger denials
Tests listed as Not Covered for a given program (eg, Medicaid, Commercial, Priority Medicare) are subject to denial for that program when billed; verify program-specific status prior to performing the test.
- Examples include PLA codes and U-codes with plan-level Not Covered annotations.
- If clinically necessary, consider individual case review and prior plan approval when applicable.
Explicit Not Covered tests are high-risk for denial
Specific tests are explicitly marked Not Covered in the listings (examples include entries across chunks); providers should not expect reimbursement for those tests and billing them will likely result in denial.
- Examples include 0279U–0281U (VWD assays) with mixed coverage and 0295U (DCISionRT) marked Not Covered.
- Check the code-level annotation and plan column before ordering.
Certain tests (e.g., 0328U) are Not Covered across plans — avoid billing
Tests explicitly designated 'Not Covered' in the document (e.g., 0328U) are listed as Not Covered for Commercial, Medicaid, and Priority Medicare and will be denied if billed under those plans.
- 0328U (definitive drug assay ≥120 drugs) is listed Not Covered across plans.
- Do not bill these codes to the listed plans; consider alternative testing or individual case review.
Verify OOS vs eC PA distinctions to determine PA need
Some tests are designated OOS for eC (No PA required) while others are eC PA; verify whether a code is OOS versus eC PA as this affects whether prior authorization is required and whether denials may occur without PA.
- Example: 0402U (Abbott Alinity m STI Assay) is OOS for eC — No PA required.
- Other tests listed as eC PA will be denied if PA is not obtained.
Billing Not Covered tests to listed plans will result in denials
Tests flagged as 'Not Covered' (multiple U-codes and CPT entries are examples) will be denied when billed under the listed plans; providers should verify coverage status and consider individual case review if clinically necessary.
Not Covered annotation indicates likely claim denial for that plan
Tests listed as 'Not Covered' for a given plan (Commercial, Medicaid, Priority Medicare) are subject to denial if billed to that plan; verify plan column and do not bill Not Covered tests to those plans.
- Examples include multiple PLA/U-codes annotated Not Covered for specific plans.
- Consider voluntary authorization or individual case review when appropriate.
OOS-for-eC 'Not Covered' codes are denial risks
Codes explicitly listed as 'OOS for eC - Not Covered' in the excerpt (examples provided) may be denied if submitted for payment under the affected plans; verify the OOS/Not Covered listing before ordering.
Investigational/experimental tests require prior plan approval for exceptions
Coverage determinations for experimental, investigational, or unproven tests may be denied unless an exception is granted via individual case review; such exceptions require prior plan approval and adjudication by a Priority Health medical director or clinical pharmacist.
- Individual case review can allow coverage for investigational yet promising care, but requires prior plan approval.
- Submit requests with full clinical justification and supporting evidence for consideration.
Not Covered / Exclusions
The policy lists a number of specific tests and test categories that are Not Covered. Examples include prenatal cfDNA screening for microdeletions and single‑gene mutations (investigational), chemosensitivity assays (experimental/investigational), and multiple proprietary or PLA tests identified in the coding tables as 'Not Covered' for the indicated plan(s). Tests annotated as 'Not Covered' in the code listings will be denied when billed under the plan(s) indicated unless an exception is granted through individual case review and prior plan approval.
Several proprietary U‑code examples are listed as Not Covered across Commercial, Medicaid, and Priority Medicare columns. Examples include 0005U, 0010U, 0040U, 0046U, 0049U, and 0055U — each shown in the coding table with a 'Not Covered' designation for the specified benefit lines.
Priority Medicare examples in the coding tables show specific CPT entries annotated 'Not Covered.' For instance, CPT codes 81240–81243 (F2, F5, FANCC, FMR1 related entries) include 'PRIORITY MEDICARE = Not Covered' annotations in the coding section; providers should follow the plan‑specific column when submitting claims.
Some single‑gene CPT codes are explicitly listed as Not Covered for certain lines of business. For example, 81324 (PMP22 duplication/deletion analysis) is annotated as 'Not Covered' for MEDICAID and PRIORITY MEDICARE in the coding tables; check the payer‑column for plan‑specific noncoverage before ordering or billing.
The policy explicitly lists specific multianalyte assays as Not Covered. One example is 81506 (PreDx Diabetes Risk Score), which is shown as not covered across Commercial, Medicaid, and Priority Medicare columns in the coding section.
Many PLA/U‑code tests are explicitly listed as Not Covered in the payer columns. Examples called out in the code tables include 0005U, 0010U, 0040U, 0046U, 0049U, 0055U; verify the specific payer column for each U‑code prior to ordering or billing.
Additional U‑code examples explicitly listed as Not Covered include 0078U, 0086U, 0115U, 0152U, 0177U and a broad set of red blood cell antigen genotyping PLA codes (eg, 0180U–0187U). These entries are annotated 'Not Covered' in the coding tables for the listed plans.
The coding tables contain a range of PLA and proprietary test codes marked in red as Not Covered for one or more plans. Providers must consult the per‑code payer column — tests flagged as 'Not Covered' will be denied if billed under that plan without an approved exception.
The document includes plan‑specific examples of tests that are not covered or have restricted coverage. For instance, several U‑codes in the 0328U–0336U and 0371U–0378U ranges are annotated as Not Covered for Commercial, Medicaid, and Priority Medicare; consult the coding listing for the exact U‑code statuses and plan columns.
Not covered entries include specific U‑codes such as 0328U, 0330U, 0371U among others shown in the code tables. These codes are annotated 'Not Covered' across the indicated plans and will be denied if submitted for payment without an approved exception.
This portion of the coding listing shows additional U‑codes annotated Not Covered, for example 0425U, 0426U, 0429U, 0463U, 0490U–0492U. Providers should verify each code’s payer column when determining coverage and prior authorization needs.
Several proprietary tests are explicitly noted as Not Covered for one or more plan types. Examples listed include 0491U, 0492U, 0500U, 0511U and others; check the per‑code plan designation before ordering or submitting claims.
A subset of commonly used CPT and other test codes are designated OOS for eC — Not Covered in the excerpt (for example, 83006, 83951, 86152, 86153, 86300, 86305, 86352), indicating those services are out‑of‑scope for the electronic prior authorization workflow and are not covered per the payer columns.
As a general principle, tests that are experimental, investigational, or unproven are excluded from coverage unless an exception is approved through individual case review. Requests for exceptions require prior plan approval and are reviewed by a Priority Health medical director or clinical pharmacist; supporting documentation must show substantial justification for coverage of an investigational test.
Eligibility Requirements & Member Applicability
Testing is indicated when there is increased risk based on documented family history, carrier status, or clinical findings consistent with a genetic disorder. For prenatal diagnostic testing, examples of indications include abnormal fetal ultrasound findings, abnormal maternal serum screening, or an increased risk based on family history or known carrier status. Pre‑ and post‑test genetic counseling and documentation of informed consent are required for medically necessary prenatal diagnostic testing.
Eligibility for coverage follows the policy’s medical necessity criteria: testing must provide direct medical benefit to the member, be ordered with appropriate clinical justification and counseling, and comply with plan and Evicore authorization requirements where applicable. Selected tests require prior authorization through Evicore; follow the Evicore criteria accessible via Priority Health Prism for required clinical information, documentation, and authorization workflow.
For testing of non‑member relatives, the policy requires that the non‑member relative’s insurer be billed and payment denied before Priority Health will consider covering testing of that relative. This step is an explicit precondition to coverage for non‑member relative testing.
Coverage of familial testing is limited: Priority Health limits coverage to testing of up to five non‑member relatives per member over the member’s lifetime, and testing must be recommended by a genetics counselor and approved by Priority Health before proceeding.
Eligibility determinations rely on appropriate documentation of counseling, indication, and prior authorization when required. Providers must document that testing will inform clinical management or provide a direct benefit to the member; otherwise testing may be considered not medically necessary.
Evicore case review may allow exceptions for tests that are otherwise investigational where sufficient supporting evidence and documentation are provided. Any exception requires prior approval and is subject to review by the payer’s clinical reviewers.
Definitions & Background
Genetic counseling is an integral part of the testing process. Genetic counseling interprets family and medical history, educates individuals about inheritance, testing options, benefits, limitations, and potential psychosocial implications, and supports informed decision‑making. The policy requires documentation of pre‑ and post‑test counseling and informed consent in accordance with Michigan law and professional guidelines; for certain indications, counseling must be performed by a board‑certified genetic counselor independent of the testing laboratory.
Coding Notes, Thresholds & Key Values
Background & Context
This policy applies to genetic counseling and genetic testing services described in the coding and coverage sections. Genetic counseling is required as part of medical necessity for many tests, and testing is intended to diagnose, guide management, or inform reproductive decisions. The policy summarizes the scope and limitations: routine counseling and tests for non‑medical purposes are excluded; specific tests require prior authorization or are designated not covered per plan‑level coding tables.
Revision History & Policy Changes
Added Policy Scope, FDA/Regulatory, Medical/Professional Society Guidelines, and Government Regulations (CMS NCDs/LCDs) sections to the document header/operational content.
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