Blue Cross Blue Shield Oklahoma prior authorization, page 18

CPT code lookup

Each row is one code from the public prior authorization list. The description is the procedure or service name on that source row. This is not a coverage decision.

Prior authorization codes

Prior authorization codes
CodeDescriptionSource
0506UGastroenterology (Barrett'S Esophagus), Esophageal Cells, Dna Methylation Analysis By Next- Generation Sequencing Of At Least 89 Differentially Methylated Genomic Regions, Algorithm Reported As Likelihood For Barrett'S Esophagus2026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 149 Original policy
0507UOncology (Ovarian), Dna, Whole- Genome Sequencing With 5- Hydroxymethylcytosine (5Hmc) Enrichment, Using Whole Blood Or Plasma, Algorithm Reported As Cancer Detected Or Not Detected2026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 149 Original policy
0508UTransplantation Medicine, Quantification Of Donor-Derived Cell- Free Dna Using 40 Single- Nucleotide Polymorphisms (Snps), Plasma, And Urine, Initial Evaluation Reported As Percentage Of Donor- Derived Cell-Free Dna With Risk For Active Rejection2026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 149 Original policy
0509UTransplantation Medicine, Quantification Of Donor-Derived Cell- Free Dna Using Up To 12 Single- Nucleotide Polymorphisms (Snps) Previously Identified, Plasma, Reported As Percentage Of Donor- Derived Cell-Free Dna With Risk For Active Rejection2026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 149 Original policy
0516UDrug Metabolism, Whole Blood, Pharmacogenomic Genotyping Of 40 Genes And Cyp2D6 Copy Number Variant Analysis, Reported As Metabolizer Status2026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 150 Original policy
0523UOncology (solid tumor), DNA, qualitative, next-generation sequencing (NGS) of singlenucleotide variants (SNV) and insertion/deletions in 22 genes utilizing formalin-fixed paraffinembedded tissue, reported as presence or absence of mutation(s), location of mutation(s), nucleotide change, and amino acid change2026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 150 Original policy
0529UHematology (venous thromboembolism [VTE]), genome- wide single-nucleotide polymorphism variants, including F2 and F5 gene analysis, and Leiden variant, by microarray analysis, saliva, report as risk score for VTE2026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 150 Original policy
0530UOncology (pan-solid tumor), ctDNA, utilizing plasma, nextgeneration sequencing (NGS) of 77 genes, 8 fusions, microsatellite instability, and tumor mutation burden, interpretative report for single-nucleotide variants, copynumber alterations, with therapy association2026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 150 Original policy
0532URare Diseases (Constitutional Disease/Hereditary Disorders), Rapid Whole Genome And Mitochondrial Dna Sequencing For Single-Nucleotide Variants, Insertions/Deletions, Copy Number Variations, Peripheral Blood, Buffy Coat, Saliva, Buccal Or Tissue Sample, Results Reported As Positive Or Negative2026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 151 Original policy
0533UDrug Metabolism (Adverse Drug Reactions And Drug Response), Genotyping Of 16 Genes (Ie, Abcg2, Cyp2B6, Cyp2C9, Cyp2C19, Cyp2C, Cyp2D6, Cyp3A5, Cyp4F2, Dpyd, G6Pd, Ggcx, Nudt15, Slco1B1, Tpmt, Ugt1A1, Vkorc1), Reported As Metabolizer Status And Transporter Function2026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 151 Original policy
0534UOncology (Prostate), Microrna, Single-Nucleotide Polymorphisms (Snps) Analysis By Rt-Pcr Of 32 Variants, Using Buccal Swab, Algorithm Reported As A Risk Score2026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 151 Original policy
0536URed Blood Cell Antigen (Fetal Rhd), Pcr Analysis Of Exon 4 Of Rhd Gene And Housekeeping Control Gene Gapdh From Whole Blood In Pregnant Individuals At 10+ Weeks Gestation Known To Be Rhd Negative, Reported As Fetal Rhd Status2026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 151 Original policy
0537UOncology (Colorectal Cancer), Analysis Of Cell-Free Dna For Epigenomic Patterns, Next- Generation Sequencing, >2500 Differentially Methylated Regions (Dmrs), Plasma, Algorithm Reported As Positive Or Negative2026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 152 Original policy
0538UOncology (Solid Tumor), Next- Generation Targeted Sequencing Analysis, Formalin-Fixed Paraffin- Embedded (Ffpe) Tumor Tissue, Dna Analysis Of 600 Genes, Interrogation For Single-Nucleotide Variants, Insertions/Deletions, Gene Rearrangements, And Copy Number Alterations, Microsatellite Instability, Tumor Mutation Burden, Reported As Actionable Variant2026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 152 Original policy
0539UOncology (Solid Tumor), Cell-Free Circulating Tumor Dna (Ctdna), 152 Genes, Next-Generation Sequencing, Interrogation For Single- Nucleotide Variants, Insertions/Deletions, Gene Rearrangements, Copy Number Alterations, And Microsatellite Instability, Using Whole-Blood Samples, Mutations With Clinical Actionability Reported As Actionable Variant2026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 152 Original policy
0540UTransplantation Medicine, Quantification Of Donor-Derived Cell- Free Dna Using Next-Generation Sequencing Analysis Of Plasma, Reported As Percentage Of Donor- Derived Cell-Free Dna To Determine Probability Of Rejection2026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 152 Original policy
0543UOncology (Solid Tumor), Next- Generation Sequencing Of Dna From Formalin-Fixed Paraffin- Embedded (Ffpe) Tissue Of 517 Genes, Interrogation For Single- Nucleotide Variants, Multi-Nucleotide Variants, Insertions And Deletions From Dna, Fusions In 24 Genes And Splice Variants In 1 Gene From Rna, And Tumor Mutation Burden2026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 153 Original policy
0544UNephrology (Transplant Monitoring), 48 Variants By Digital Pcr, Using Cell-Free Dna From Plasma, Donor- Derived Cell-Free Dna, Percentage Reported As Risk Rejection2026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 153 Original policy
0549UOncology (Urothelial), Dna, Quantitative Methylated Real-Time Pcr Of Trna-Cys, Sim2, And Nkx1-1, Using Urine, Diagnostic Algorithm Reported As A Probability Index For Bladder Cancer And/Or Upper Tract Urothelial Carcinoma (Utuc)2026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 153 Original policy
0552UReproductive medicine (preimplantation genetic assessment), analysis for known genetic disorders from trophectoderm biopsy, linkage analysis of disease-causing locus, and when possible, targeted mutation analysis for known familial variant, reported as low-risk or high- risk for familial genetic disorder2026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 153 Original policy
0553UReproductive medicine (preimplantation genetic assessment), analysis of 24 chromosomes using DNA genomic sequence analysis from embryonic trophectoderm for structural rearrangements, aneuploidy, and a mitochondrial DNA score, results reported as normal/balanced (euploidy/balanced), unbalanced structural rearrangement, monosomy, trisomy, segmental aneuploidy, or mosaic, per embryo tested2026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 154 Original policy
0554UReproductive medicine (preimplantation genetic assessment), analysis of 24 chromosomes using DNA genomic sequence analysis from trophectoderm biopsy for aneuploidy, ploidy, a mitochondrial DNA score, and embryo quality control, results reported as normal (euploidy), monosomy, trisomy, segmental aneuploidy, triploid, haploid, or mosaic, with quality control results reported as contamination detected or inconsistent cohort when applicable, per embryo tested2026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 154 Original policy
0555UReproductive medicine (preimplantation genetic assessment), analysis of 24 chromosomes using DNA genomic sequence analysis from embryonic trophectoderm for structural rearrangements, aneuploidy, ploidy, a mitochondrial DNA score, and embryo quality control, results reported as normal/balanced (euploidy/balanced), unbalanced structural rearrangement, monosomy, trisomy, segmental aneuploidy, triploid, haploid, or mosaic, with quality control results reported as contamination detected or inconsistent cohort when applicable, per embryo tested2026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 155 Original policy
0560UOncology (minimal residual disease [MRD]), genomic sequence analysis, cell-free DNA, whole blood and tumor tissue, baseline assessment for design and construction of a personalized variant panel to evaluate current MRD and for comparison to subsequent MRD assessments2026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 155 Original policy
0561UOncology (minimal residual disease [MRD]), genomic sequence analysis, cell-free DNA, whole blood, subsequent assessment with comparison to initial assessment to evaluate for MRD2026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 155 Original policy
0562UOncology (solid tumor), targeted genomic sequence analysis, 33 genes, detection of single-nucleotide variants (SNVs), insertions and deletions, copy-number amplifications, and translocations in human genomic circulating cell-free DNA, plasma, reported as presence of actionable variants2026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 156 Original policy
0565UOncology (hepatocellular carcinoma), next-generation sequencing methylation pattern assay to detect 6626 epigenetic alterations, cell-free DNA, plasma, algorithm reported as cancer signal detected or not detected2026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 156 Original policy
0566UOncology (lung), qPCR-based analysis of 13 differentially methylated regions (CCDC181, HOXA7, LRRC8A, MARCHF11, MIR129-2, NCOR2, PANTR1, PRKCB, SLC9A3, TBR1_2, TRAP1, VWC2, ZNF781), pleural fluid, algorithm reported as a qualitative result2026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 156 Original policy
0567URare diseases (constitutional/heritable disorders), whole-genome sequence analysis combination of short and long reads, for single-nucleotide variants, insertions/deletions and characterized intronic variants, copy- number variants, duplications/deletions, mobile element insertions, runs of homozygosity, aneuploidy, and inversions, mitochondrial DNA sequence and deletions, short tandem repeat genes, methylation status of selected regions, blood, saliva, amniocentesis, chorionic villus sample or tissue, identification and categorization of genetic variants2026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 157 Original policy
0569UOncology (solid tumor), next- generation sequencing analysis of tumor methylation markers (>20000 differentially methylated regions) present in cell-free circulating tumor DNA (ctDNA), whole blood, algorithm reported as presence or absence of ctDNA with tumor fraction, if appropriate2026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 157 Original policy
0571UOncology (solid tumor), DNA (80 genes) and RNA (10 genes), by next- generation sequencing, plasma, including single-nucleotide variants, insertions/deletions, copy-number alterations, microsatellite instability, and fusions, reported as clinically actionable variants2026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 157 Original policy
G9143Warfarin Responsiveness Testing By Genetic Technique Using Any Method Any Number Of Specimen(S)2026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 158 Original policy
S3800Genetic Testing For Amyotrophic Lateral Sclerosis (Als)2026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 158 Original policy
S3840Dna Analysis For Germline Mutations Of The Ret Proto- Oncogene For Susceptibility To Multiple Endocrine Neoplasia Type 22026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 158 Original policy
S3841Genetic Testing For Retinoblastoma2026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 158 Original policy
S3842Genetic Testing For Von Hippel- Lindau Disease2026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 158 Original policy
S3844Dna Analysis Of The Connexin 26 Gene (Gjb2) For Susceptibility To Congenital Profound Deafness2026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 158 Original policy
S3845Genetic Testing For Alpha- Thalassemia2026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 158 Original policy
S3846Genetic Testing For Hemoglobin E Beta-Thalassemia2026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 158 Original policy
S3849Genetic Testing For Niemann-Pick Disease2026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 158 Original policy
S3850Genetic Testing For Sickle Cell Anemia2026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 158 Original policy
S3852Dna Analysis For Apoe Epsilon 4 Allele For Susceptibility To Alzheimer'S Disease2026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 158 Original policy
S3853Genetic Testing For Myotonic Muscular Dystrophy2026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 158 Original policy
S3854Gene Expression Profiling Panel For Use In The Management Of Breast Cancer Treatment2026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 158 Original policy
S3861Genetic Testing Sodium Channel Voltage-Gated Type V Alpha Subunit (Scn5A) And Variants For Suspected Brugada Syndrome2026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 158 Original policy
S3865Comprehensive Gene Sequence Analysis For Hypertrophic Cardiomyopathy2026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 159 Original policy
S3866Genetic Analysis For A Specific Gene Mutation For Hypertrophic Cardiomyopathy (Hcm) In An Individual With A Known Hcm Mutation In The Family2026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 159 Original policy
S3870Comparative Genomic Hybridization (Cgh) Microarray Testing For Developmental Delay Autism Spectrum Disorder And/Or Intellectual Disability2026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 159 Original policy
20930Allograft Morselized Or Placement Of Osteopromotive Material For Spine Surgery Only (List Separately In Addition To Code For Primary Procedure)2026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 159 Original policy
20931Allograft Structural For Spine Surgery Only (List Separately In Addition To Code For Primary Procedure)2026 Commercial Outpatient Medical Surgical Fully Insured Prior Authorization Codes, Pg 159 Original policy

Sources

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The information provided on this page is for general informational purposes only and does not constitute billing, coding, or reimbursement advice. Nothing on this page should be relied upon as a substitute for clinician assessment, professional billing guidance, or as a definitive statement of any payor's billing requirements or policies.

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