Description
This code is used for testing patient specimens to identify genetic duplications and deletions in at least five specific genes associated with hereditary breast cancer. The results can provide critical insights into the risk of developing related disorders due to alterations in DNA.
No crosswalks found.
No alternates found.
No codes found here.
We make no claims to ownership of the coding systems referenced on this platform. Codes and descriptions are produced from claims and chargemaster data available through the CMS-9915-F Transparency in Coverage Final Rule and via state or federal datasets. This service is provided solely as a reference to encourage use of these codes in our chargemaster review and automated billing tools, so that healthcare professionals can understand and correctly report these codes in their claims.