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 93201-2: Coronary heart disease multigene analysis Molgen Doc (Bld/Tiss)

Name: LOINC Code 93201-2: Coronary heart disease multigene analysis Molgen Doc (Bld/Tiss)
Creator: HealthAssure Clinical Team
Published: 2026-05-21T09:00:22.239Z

93201-2 is a LOINC code used to identify Coronary heart disease multigene 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 Coronary heart disease multigene 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 Coronary heart disease multigene 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

Coronary heart disease multigene analysis in Blood or Tissue by Molecular genetics method

Coronary heart disease multigene analysis

This test includes analysis of alleles at multiple genetic loci associated with coronary heart disease (CHD). Testing is performed to determine an individual's genetic-based risk for CHD, particularly in patients at intermediate risk for atherosclerotic cardiovascular disease (ASCVD) and those with family history of ASCVD. An overall genetic risk score (GRS) [LOINC93306-9] and interpretation (high/low) [LOINC: 93307-7] may be provided to improve risk estimates and aid in the prevention of CHD. The GRS is based on the genotype of multiple genetic variants associated with CHD. Additionally, a patient's overall 10-year probability of CHD may be calculated by multiply the 10-year ASCVD score from the Pooled Cohort Equations by the GRS.

Blood; CHD Multigene Anl; Dis; Diseases; Document; Dz; Finding; Findings; Gene; Gene panel; Molecular genetics; Molecular pathology; MOLPATH; Multi-gene study; Multiple-gene panel test; PCR; Point in time; Random; 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

Coronary heart disease multigene analysis Molgen Doc (Bld/Tiss)Coronary heart disease multigene analysis in Blood or Tissue by Molecular genetics methodCHD Multigene Anl Bld/TCoronary heart disease multigene analysisMOLPATHCoronary heart disease multigene analysis, Blood or tissue specimenFind

Frequently asked questions

Code details

Code93201-2

SystemLOINC

Display nameCoronary heart disease multigene analysis Molgen Doc (Bld/Tiss)

DescriptionCoronary heart disease multigene analysis

Short nameCHD Multigene Anl Bld/T

ComponentCoronary heart disease multigene analysis

PropertyFind

TimingPt

System (specimen)Bld/Tiss

ScaleDoc

MethodMolgen

ClassMOLPATH

StatusACTIVE

Order/ObservationBoth

Flags

BillableNo

Valid clinical useNo

Source

SourceLOINC

Version2.82

Releasemain

First released2.67

Last changed2.67

Consumer names

Coronary heart disease multigene analysis, Blood or tissue specimen

Part names

Coronary heart disease multigene analysisFindPtBld/TissDocMolgenFindingPoint 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.