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.

LOINCActiveObservation

LOINC Code 51652-6: SLC14A1 gene targeted mutation analysis Molgen Nom (Bld/Tiss)

Name: LOINC Code 51652-6: SLC14A1 gene targeted mutation analysis Molgen Nom (Bld/Tiss)
Creator: HealthAssure Clinical Team
Published: 2026-05-21T08:59:35.012Z

51652-6 is a LOINC code used to identify SLC14A1 gene targeted mutation analysis Molgen Nom (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 SLC14A1 gene targeted 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 SLC14A1 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: Observation
Method: Molgen

What it does not mean

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

Key facts

SLC14A1 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal
SLC14A1 gene targeted mutation analysis
Blood; FLJ33745; FLJ41687; Genetics; Heredity; Heritable; HsT1341; HUT11; Identity or presence; Inherited; JK; Kidd; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; Nominal; PCR; Point in time; RACH1; RACH2; Random; solute carrier family 14 (urea transporter), member 1 (Kidd blood group); Tissue; Tissue, unspecified; UT1; UT-B1; UTE; 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

SLC14A1 gene targeted mutation analysis Molgen Nom (Bld/Tiss)SLC14A1 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method NominalSLC14A1 gene Mut Anl Bld/TSLC14A1 gene targeted mutation analysisMOLPATH.MUTSLC14A1 gene targeted mutation analysis, Blood or tissue specimenPrid

Frequently asked questions

Code details

Code51652-6

SystemLOINC

Display nameSLC14A1 gene targeted mutation analysis Molgen Nom (Bld/Tiss)

DescriptionSLC14A1 gene targeted mutation analysis

Short nameSLC14A1 gene Mut Anl Bld/T

ComponentSLC14A1 gene targeted mutation analysis

PropertyPrid

TimingPt

System (specimen)Bld/Tiss

ScaleNom

MethodMolgen

ClassMOLPATH.MUT

StatusACTIVE

Order/ObservationObservation

Flags

BillableNo

Valid clinical useNo

Source

SourceLOINC

Version2.82

Releasemain

First released2.24

Last changed2.63

Consumer names

SLC14A1 gene targeted mutation analysis, Blood or tissue specimen

Part names

SLC14A1 gene targeted mutation analysisPridPtBld/TissNomMolgenPresence or IdentityPoint 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.