VKORC1 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal   50722-8

LOINC Code


LOINC code50722-8
nameVKORC1 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal
descriptionThe presence of the heterozygous missense mutation -1639 G>A in the VKORC1 gene can result in warfarin resistance. VKORC1 DNA analysis is performed by PCR followed by restriction enzyme digestion to detect -1639 G>A.
statusACTIVE

Fully-Specified Name

componentVKORC1 gene targeted mutation analysis
propertyPrid  =  Presence or identity:  Prid stands for “Presence or identity”, is used for assays that detect whether or not an analyte of a particular kind is present, and if it is, to identify the specific analyte.
timePt  =  Point in time:  To identify measures at a point in time. This is a synonym for “spot” or “random” as applied to urine measurements.
systemBld/Tiss
    Bld  =  Whole blood
    Tiss  =  Tissue, unspecified
scaleNom  =  Nominal:  Nominal or categorical responses that do not have a natural ordering. (e.g., names of bacteria, reported as answers, categories of appearance that do not have a natural ordering, such as, yellow, clear, bloody.
methodMolgen  =  Molecular Genetics:  General class of methods used to detect genetic attributes on a molecular basis including RFL, PCR and other methods.

Additional Names

short nameVKORC1 gene Mut Anl Bld/T

Basic Attributes

classMOLPATH.PHARMG
type1  Laboratory
order vs. observationBoth

Associated Observations

LOINC codes that represent optional associated observation(s) for a clinical observation or laboratory test. A LOINC term may represent a single associated observation or panel containing several associated observations.

Member of these Panels

54450-2CYP2C9 and VKORC1 panel - Blood or Tissue by Molecular genetics method
93196-4Warfarin response genotype panel - Blood or Tissue by Molecular genetics method

History/Usage

test rank13213 of 2000 most commonly performed tests by labs in USA
first released
last updated2.73
last change typeMIN  - change to field other than name
change reasonRelease 2.67: CLASS: Updated to MOLPATH.PHARMG, the more representative LOINC Class for this concept.; Previous Releases: Based on LOINC Committee review (June 2016), "targeted" was added to the Component to clarify that this test is looking for a specific set of mutations as described in the LOINC User Guide under the Molecular Genetics section.

Related Names

Blood
EDTP308
Genetics
Heredity
Heritable
Identity or presence
IMAGE3455200
Inherited
Molecular genetics
Molecular pathology
MOLPATH
MOLPATH.PHARMG
MST134
MST576
Mut
Mut Anl
Mutations
Nominal
PCR
Point in time
Random
Tissue
Tissue, unspecified
vitamin K epoxide reductase complex, subunit 1
VKCFD2
VKOR
WB
Whole blood
Whole blood or Tissue

Copyright © 2023 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © 1995-2023, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. See https://loinc.org/license for the full LOINC copyright and license.

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