This page is part of the FHIR Specification (v1.6.0: STU 3 Ballot 4). The current version which supercedes this version is 5.0.0. For a full list of available versions, see the Directory of published versions 

This is a value set defined by the FHIR project.
Summary
| Defining URL: | http://hl7.org/fhir/ValueSet/LOINC-53037-8-answerlist |
| Name: | LOINC 53037-8 answerlist |
| Definition: | LOINC answer list for Genetic disease sequence variation interpretation |
| Committee: | Orders and Observations Work Group |
| OID: | 2.16.840.1.113883.4.642.2.511 (for OID based terminology systems) |
| Copyright: | This content LOINC® is copyright © 1995 Regenstrief Institute, Inc. and the LOINC Committee, and available at no cost under the license at http://loinc.org/terms-of-use |
| Source Resource | XML / JSON |
This value set is not currently used

This value set includes codes from the following code systems:
| Code | Display | |
| LA6668-3 | Pathogenic | |
| LA6669-1 | Presumed pathogenic | |
| LA6682-4 | Unknown significance | |
| LA6675-8 | Benign | |
| LA6674-1 | Presumed benign |
See the full registry of value sets defined as part of FHIR.
Explanation of the columns that may appear on this page:
| Level | A few code lists that FHIR defines are hierarchical - each code is assigned a level. In this scheme, some codes are under other codes, and imply that the code they are under also applies |
| Source | The source of the definition of the code (when the value set draws in codes defined elsewhere) |
| Code | The code (used as the code in the resource instance) |
| Display | The display (used in the display element of a Coding). If there is no display, implementers should not simply display the code, but map the concept into their application |
| Definition | An explanation of the meaning of the concept |
| Comments | Additional notes about how to use the code |