LOINC Code 99057-2: SLC12A1 gene full mutation analysis Molgen Doc (Bld)

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 SLC12A1 gene full mutation analysis. It is commonly used with the system or sample type Bld.

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

• SLC12A1 gene full mutation analysis in Blood by Molecular genetics method
• SLC12A1 gene full mutation analysis
• Blood; BSC1 gene; Document; Finding; Findings; full gene sequencing; Full Mut Anl; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mutations; NKCC2 gene; PCR; Point in time; Random; sequencing of entire coding region; WB; Whole blood

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