LOINC Home

{component}   LP432695-7

Laboratory   LP29693-6

Lab terms not yet categorized   LP248770-2

CYP4F2 gene c.1297G>A [Genotype] in Blood or Tissue by Molecular genetics method Nominal   93197-2

LOINC Code


LOINC code93197-2
nameCYP4F2 gene c.1297G>A [Genotype] in Blood or Tissue by Molecular genetics method Nominal
descriptionThe presence of the CYP4F2*3 (rs2108622) allele indicates that a patient who self-identifies as being of non-African ancestry may require a slightly increased warfarin dose than predicted by CYP2C9/VKORC1 alone.[PMID: 18250228] The rs2108622 variant (c.1297G>A) results in an amino acid substitution (valine to methionine) at position 433 (p.V433M).
statusACTIVE

Fully-Specified Name

componentCYP4F2 gene.c.1297G>A
propertyGeno  =  Genotype
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 nameCYP4F2 c.1297G>A Geno Bld/T

Basic Attributes

classMOLPATH.PHARMG
type1  Laboratory
order vs. observationObservation

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

93196-4Warfarin response genotype panel - Blood or Tissue by Molecular genetics method

History/Usage

first released
last updated2.68
last change typeMIN  - change to field other than name

Related Names

Blood
CYP4F2 c.1297G>
A
Molecular genetics
Molecular pathology
MOLPATH
MOLPATH.PHARMG
NC_000019.10:g.15879621C>
T
NC_000019.9:g.15990431C>
T
NG_007971.2:g.23454G>
A
NM_001082.4:c.1297G>
A
Nominal
NP_001073.3:p.Val433Met
p.V433M
PCR
Point in time
Random
rs2108622
Tissue
Tissue, unspecified
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.

demo
request yours today
 subscribe
start today
 newsletter
free subscription

Thank you for choosing Find-A-Code, please Sign In to remove ads.