LOINC Code 89038-4: CHEK2 gene del+dup and full mutation analysis Molgen Doc (Bld/Tiss)

What is this code?

LOINC codes identify tests, measurements, observations, survey items, and clinical questions in a standardized way. It is associated with the component CHEK2 gene deletion+duplication & full mutation analysis. It is commonly used with the system or sample type Bld/Tiss.

When is it used?

• Used in lab systems, EHRs, and clinical data exchange.
• May identify a test, observation, survey item, or clinical document request rather than a diagnosis.
• Status: ACTIVE
• Order vs observation: Both
• Method: Molgen

What it does not mean

• The code identifies the observation or test, not the actual result.

Key facts

• CHEK2 gene deletion+duplication and full mutation analysis in Blood or Tissue by Molecular genetics method
• CHEK2 gene deletion+duplication & full mutation analysis
• Amplification; Blood; CDS1; checkpoint kinase 2; CHK2; Del; Del+Dup; Del+Dup + Full Mut Anl; Deletions; Document; Dp; Finding; Findings; full gene sequencing; Full Mut Anl; Genetics; hCds1; Heredity; Heritable; HuCds1; Inherited; LFS2; Li-Fraumeni syndrome; Li-Fraumeni syndrome 2; Molecular genetics; Molecular pathology; MOLPATH; Mut; Mutations; PCR; Point in time; PP1425; RAD53; Random; sequencing of entire coding region; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue

Where you may see this code

You may see this code in lab systems, lab reports, EHR exports, interoperability feeds, or other structured clinical data exchanges.

Common synonyms

Frequently asked questions