LOINC Code 21735-6: SNCA gene targeted mutation analysis Molgen 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 SNCA 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: Molgen

What it does not mean

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

Key facts

• SNCA gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal
• SNCA gene targeted mutation analysis
• Blood; Genetics; Heredity; Heritable; Identity or presence; Inherited; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; NACP; Nominal; Non A4 component of amyloid precursor; PARK1; PARK4; Parkinson disease; PCR; PD1; Point in time; Random; Synuclein, alpha; synuclein, alpha (non A4 component of amyloid precursor); 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