S3861
HCPCSGenetic test brugada
Official HCPCS Level II long descriptor
Genetic testing, sodium channel, voltage-gated, type v, alpha subunit (scn5a) and variants for suspected brugada syndrome
HCPCS Level II code S3861 is maintained by CMS and is active in the current quarterly release.
Short descriptor
Genetic test brugada
Added to HCPCS: 2008-10-01
Nearby codes in S3
- S3844Dna analysis deafness
- S3845Gene test alpha-thalassemia
- S3846Gene test beta-thalassemia
- S3849Gene test niemann-pick
- S3850Gene test sickle cell
- S3852Dna analysis apoe alzheimer
- S3853Gene test myo musclr dyst
- S3854Gene profile panel breast
- S3865Comp genet test hyp cardiomy
- S3866Spec gene test hyp cardiomy
- S3870Cgh test developmental delay
- S3900Surface emg
- S3902Ballistocardiogram
- S3904Masters two step
Where this code sits
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HCPCS Level II July 2026 quarterly update. Centers for Medicare & Medicaid Services (CMS), “July 2026 Alpha-Numeric HCPCS File” (HCPC2026_JUL_ANWEB_06172026.txt). Download the original file from cms.gov. Public domain (US Government work). Descriptors, billable flags and instructional notes on this page are reproduced from that file without modification. Krasyn adds no clinical guidance.