What does this LOINC code represent?

This LOINC code identifies a lab observation, measurement, question, or clinical concept in a standardized format.

Is this enough to understand my test result?

No. The code identifies the test or observation, but the interpretation depends on the actual result, reference range, and clinical context.

LOINCActiveBoth

LOINC Code 94216-9: STK11 gene del+dup and full mutation analysis Molgen Doc (Bld/Tiss)

Name: LOINC Code 94216-9: STK11 gene del+dup and full mutation analysis Molgen Doc (Bld/Tiss)
Creator: HealthAssure Clinical Team
Published: 2026-05-21T09:00:24.119Z

94216-9 is a LOINC code used to identify STK11 gene del+dup and full mutation analysis Molgen Doc (Bld/Tiss) in laboratory and clinical observation data. You may see this code in lab systems, lab reports, EHR exports, interoperability feeds, or other structured clinical data exchanges. LOINC codes identify tests, measurements, observations, survey items, and clinical questions in a standardized way. It is associated with the component STK11 gene deletion+duplication & full mutation analysis. It is commonly used with the system or sample type Bld/Tiss.

Reviewed by HealthAssure Clinical TeamUpdated 21 May 2026

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 STK11 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

STK11 gene deletion+duplication and full mutation analysis in Blood or Tissue by Molecular genetics method

STK11 gene deletion+duplication & full mutation analysis

Test includes full sequence analysis (e.g. by Sanger and/or next-generation sequencing) and deletion/duplication analysis for the detection of variants and large deletions/duplications in the STK11 gene to confirm a diagnosis of Peutz-Jeghers syndrome (PJS), an autosomal dominant disorder characterized by hamartomatous polyps in the gastrointestinal tract, pigmented macules on the skin and mouth, and other neoplasms.[GHR geneSTK11]

Amplification; Blood; Del; Del+Dup; Del+Dup + Full Mut Anl; Deletions; Document; Dp; Finding; Findings; full gene sequencing; Full Mut Anl; Genetics; Heredity; Heritable; hLKB1; Inherited; LKB1; Molecular genetics; Molecular pathology; MOLPATH; Mut; Mutations; PCR; PJS; Point in time; Random; sequencing of entire coding region; serine/threonine kinase 11; 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

STK11 gene del+dup and full mutation analysis Molgen Doc (Bld/Tiss)STK11 gene deletion+duplication and full mutation analysis in Blood or Tissue by Molecular genetics methodSTK11 gene Del+Dup + Full Mut Anl Bld/TSTK11 gene deletion+duplication & full mutation analysisMOLPATHSTK11 gene variant analysis, Blood or tissue specimenFind

Frequently asked questions

Code details

Code94216-9

SystemLOINC

Display nameSTK11 gene del+dup and full mutation analysis Molgen Doc (Bld/Tiss)

DescriptionSTK11 gene deletion+duplication & full mutation analysis

Short nameSTK11 gene Del+Dup + Full Mut Anl Bld/T

ComponentSTK11 gene deletion+duplication & full mutation analysis

PropertyFind

TimingPt

System (specimen)Bld/Tiss

ScaleDoc

MethodMolgen

ClassMOLPATH

StatusACTIVE

Order/ObservationBoth

Flags

BillableNo

Valid clinical useNo

Source

SourceLOINC

Version2.82

Releasemain

First released2.68

Last changed2.68

Consumer names

STK11 gene variant analysis, Blood or tissue specimen

Part names

STK11 gene deletion+duplication & full mutation analysisFindPtBld/TissDocMolgenSTK11 gene deletion+duplication and full mutation analysisFindingPoint in time (spot)Blood or TissueMolecular genetics

About this content

This page is prepared by HealthAssure's clinical team using official coding standards from LOINC. AI tools assist with drafting explanations, which are then reviewed and verified by healthcare professionals for accuracy. This content is for informational purposes and does not replace professional medical advice. Meet our team.