LOINC Code 107252-9: CSF3R gene targeted mutation analysis Sequencing Nom (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 CSF3R gene targeted 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: Sequencing

What it does not mean

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

Key facts

• CSF3R gene mutations found [Identifier] in Blood or Tissue by Sequencing Nominal
• CSF3R gene targeted mutation analysis
• Blood; CD114; colony stimulating factor 3 receptor; GCSFR; high-throughput sequencing; HTS; Identity or presence; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; Next generation sequencing; NGS; Nominal; Point in time; Random; SCN7; 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