LOINC Code 41268-4: VWF gene.p.Thr791Met Molgen Ql (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 VWF gene.p.Thr791Met. 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

• VWF gene.p.Thr791Met [Presence] in Blood by Molecular genetics method
• VWF gene.p.Thr791Met
• Blood; F8VWF; Genetics; Heredity; Heritable; Inherited; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Ordinal; P prime; PCR; Point in time; PR; QL; Qual; Qualitative; Random; rs61748477; Screen; T28M; Thr791Met; von Willebrand factor; von Willebrand Factor gene; VWD; VWF p.T791M; 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