List With HCPCS Codes For Genetic Testing

The HCPCS codes for Genetic Testing (S3800-S3870) cover a wide range of tests that help identify genetic mutations and disorders. These codes include tests for conditions such as amyotrophic lateral sclerosis (ALS), multiple endocrine neoplasia type 2, retinoblastoma, Von Hippel-Lindau disease, congenital deafness, alpha-thalassemia, sickle cell anemia, Alzheimer’s disease, myotonic muscular dystrophy, breast cancer treatment management, brugada syndrome, hypertrophic cardiomyopathy, and developmental delay, autism spectrum disorder, and intellectual disability.

1. HCPCS Code S3800

HCPCS S3800 describes genetic testing for amyotrophic lateral sclerosis (ALS).

2. HCPCS Code S3840

HCPCS S3840 describes DNA analysis for germline mutations of the RET proto-oncogene for susceptibility to multiple endocrine neoplasia type 2.

3. HCPCS Code S3841

HCPCS S3841 describes genetic testing for retinoblastoma.

4. HCPCS Code S3842

HCPCS S3842 describes genetic testing for Von Hippel-Lindau disease.

5. HCPCS Code S3844

HCPCS S3844 describes DNA analysis of the connexin 26 gene (GJB2) for susceptibility to congenital, profound deafness.

6. HCPCS Code S3845

HCPCS S3845 describes genetic testing for alpha-thalassemia.

7. HCPCS Code S3846

HCPCS S3846 describes genetic testing for hemoglobin E beta-thalassemia.

8. HCPCS Code S3849

HCPCS S3849 describes genetic testing for Niemann-Pick disease.

9. HCPCS Code S3850

HCPCS S3850 describes genetic testing for sickle cell anemia.

10. HCPCS Code S3852

HCPCS S3852 describes DNA analysis for APOE epsilon 4 allele for susceptibility to Alzheimer’s disease.

11. HCPCS Code S3853

HCPCS S3853 describes genetic testing for myotonic muscular dystrophy.

12. HCPCS Code S3854

HCPCS S3854 describes a gene expression profiling panel for use in the management of breast cancer treatment.

13. HCPCS Code S3861

HCPCS S3861 describes genetic testing for sodium channel, voltage-gated, type V, alpha subunit (SCN5A) and variants for suspected Brugada syndrome.

14. HCPCS Code S3865

HCPCS S3865 describes comprehensive gene sequence analysis for hypertrophic cardiomyopathy.

15. HCPCS Code S3866

HCPCS S3866 describes genetic analysis for a specific gene mutation for hypertrophic cardiomyopathy (HCM) in an individual with a known HCM mutation in the family.

16. HCPCS Code S3870

HCPCS S3870 describes comparative genomic hybridization (CGH) microarray testing for developmental delay, autism spectrum disorder, and/or intellectual disability.