CYP4F2 gene c.1297G>A [Genotype] in Blood or Tissue by Molecular genetics method Nominal 93197-2
LOINC Code
| LOINC code | 93197-2 | ||
|---|---|---|---|
| name | CYP4F2 gene c.1297G>A [Genotype] in Blood or Tissue by Molecular genetics method Nominal | ||
| description | The 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). | ||
| status | ACTIVE | ||
Fully-Specified Name | |||
| component | CYP4F2 gene.c.1297G>A | ||
| property | Geno = Genotype | ||
| time | Pt = Point in time: To identify measures at a point in time. This is a synonym for “spot” or “random” as applied to urine measurements. | ||
| system | Bld/Tiss Bld = Whole blood Tiss = Tissue, unspecified | ||
| scale | Nom = 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. | ||
| method | Molgen = Molecular Genetics: General class of methods used to detect genetic attributes on a molecular basis including RFL, PCR and other methods. | ||
Additional Names | |||
| short name | CYP4F2 c.1297G>A Geno Bld/T | ||
Basic Attributes | |||
| class | MOLPATH.PHARMG | ||
| type | 1 Laboratory | ||
| order vs. observation | Observation | ||
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 | |||
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History/Usage | |||
| first released | |||
| last updated | 2.68 | ||
| last change type | MIN - change to field other than name | ||
Related Names | |||
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