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ALL MEDICAL CODES IN CATEGORY Genetic Analysis Procedures
2025 CPT code 81301
Microsatellite instability analysis to detect mismatch repair deficiency, including comparison of neoplastic and normal tissue if performed.
2025 CPT code 81292
Complete gene sequencing analysis of the MLH1 gene.
2025 CPT code 81216
Analysis of the complete BRCA2 gene sequence.
2025 CPT code 81252
Analysis of the complete GJB2 gene sequence, encompassing all exons and introns, to identify variations associated with hearing loss.
2025 CPT code 81233
Analysis of the Bruton's tyrosine kinase (BTK) gene for common variants (e.g., C481S, C481R, C481F).
2025 CPT code 81166
Analysis of the BRCA1 gene for full duplication/deletion to detect large gene rearrangements.
2025 CPT code 81320
Analysis of common variants in the PLCG2 gene.
2025 CPT code 81312
Analysis of the PABPN1 gene to detect abnormal alleles, often used in diagnosing oculopharyngeal muscular dystrophy (OPMD).
2025 CPT code 81300
Analysis of the MSH6 gene for duplications and deletions.
2025 CPT code 81321
Complete gene sequencing analysis of the PTEN gene.
2025 CPT code 81302
Analysis of the full sequence of the MECP2 gene.
2025 CPT code 81220
Analysis of the cystic fibrosis transmembrane conductance regulator (CFTR) gene for common variants, typically using ACMG/ACOG guidelines.
2025 CPT code 81120
Analysis of common variants in the IDH1 gene, including R132H and R132C,typically used in glioma diagnosis.
2025 CPT code 81232
Analysis of common variants in the dihydropyrimidine dehydrogenase (DPYD) gene (e.g., *2A, *4, *5, *6) to assess drug metabolism, primarily for 5-fluorouracil (5-FU) and capecitabine.
2025 CPT code 81242
Analysis of the FANCC gene for common variants, such as IVS4+4A>T, associated with Fanconi anemia.
2025 CPT code 81317
Analysis of the entire PMS2 gene sequence.
2025 CPT code 81248
Analysis of known familial variants in the glucose-6-phosphate dehydrogenase (G6PD) gene.
2025 CPT code 81202
Analysis of known familial variants in the adenomatous polyposis coli (APC) gene.
2025 CPT code 81355
Analysis of VKORC1 gene for common variants related to warfarin metabolism.
2025 CPT code 81172
AFF2 (ALF transcription elongation factor 2 [FMR2]) (eg, fragile X intellectual disability 2 [FRAXE]) gene analysis; characterization of alleles (eg, expanded size and methylation status).
2025 CPT code 81328
Analysis of the SLCO1B1 gene for common variants (e.g., *5).
2025 CPT code 81333
Analysis of the transforming growth factor beta-induced gene (TGFBI), common variants (e.g., R124H, R124C, R124L, R555W, R555Q).
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