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 94402-5: ANKK1 gene c.2137G>A genotype Molgen (Bld/Tiss)

Name: LOINC Code 94402-5: ANKK1 gene c.2137G>A genotype Molgen (Bld/Tiss)
Creator: HealthAssure Clinical Team
Published: 2026-05-21T09:00:24.120Z

94402-5 is a LOINC code used to identify ANKK1 gene c.2137G>A genotype Molgen (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 ANKK1 gene.c.2137G>A. 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 ANKK1 gene.c.2137G>A. 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

ANKK1 gene c.2137G>A [Genotype] in Blood or Tissue by Molecular genetics method Nominal

ANKK1 gene.c.2137G>A

The patient's genotype for the DRD2/ANKK1 Taq1A polymorphism (rs1800497, Glu713Lys, c.2137G>A) variant in the ANKK1 (Ankyrin repeat and kinase domain containing 1) gene. This variant is associated with reduced striatal D2/3 receptor binding in healthy individuals as well as depression and addiction.[PMID23683269]

ANKK1 c.2137G>A; Blood; DRD2/ANKK1 Taq1A polymorphism; Genetics; Glu713Lys; Heredity; Heritable; Inherited; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.PHARMG; NM_178510.2(ANKK1)c.2137G>A (p.Glu713Lys); Nominal; PCR; Point in time; Random; rs1800497; 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

ANKK1 gene c.2137G>A genotype Molgen (Bld/Tiss)ANKK1 gene c.2137G>A [Genotype] in Blood or Tissue by Molecular genetics method NominalANKK1 c.2137G>A Geno Bld/TANKK1 gene.c.2137G>AMOLPATH.PHARMGANKK1 gene c.2137G>A genotype, Blood or tissue specimenGeno

Frequently asked questions

Code details

Code94402-5

SystemLOINC

Display nameANKK1 gene c.2137G>A genotype Molgen (Bld/Tiss)

DescriptionANKK1 gene.c.2137G>A

Short nameANKK1 c.2137G>A Geno Bld/T

ComponentANKK1 gene.c.2137G>A

PropertyGeno

TimingPt

System (specimen)Bld/Tiss

ScaleNom

MethodMolgen

ClassMOLPATH.PHARMG

StatusACTIVE

Order/ObservationObservation

Flags

BillableNo

Valid clinical useNo

Source

SourceLOINC

Version2.82

Releasemain

First released2.68

Last changed2.68

Consumer names

ANKK1 gene c.2137G>A genotype, Blood or tissue specimen

Part names

ANKK1 gene.c.2137G>AGenoPtBld/TissNomMolgenANKK1 gene c.2137G>AGenotypePoint 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.