LP185975-2
CYP1A2 gene.c.-3860G>A
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Description
The CYP1A2 gene variant -3860G>A is inherited in an autosomal recessive fashion and associated with lower inducibility in Asians but increased inducibility in Northern Europeans. Individuals who are homozygous or compound heterozygous for polymorphisms in the CYP1A2 gene are poor metabolizers. Patients who are heterozygous, having 1 normal gene and 1 defective variant, will have metabolism intermediate between the extensive (normal) and poor metabolizers. Source: Regenstrief LOINC
Basic Part Properties
- Part Display Name
- CYP1A2 gene c.-3860G>A
- Part Type
- Component (Describes the core component or analyte measured)
- Created On
- 2014-09-18
- Construct for LOINC Short Name
- CYP1A2 c.-3860G>A
LOINC Terminology Service (API) using HL7® FHIR® Get Info
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- CodeSystem lookup
- https:
//fhir.loinc.org/CodeSystem/$lookup?system=http: //loinc.org&code=LP185975-2
Language Variants Get Info
| Tag | Language | Translation |
|---|---|---|
| zh-CN | Chinese (China) | CYP1A2 基因.c.-3860G>A |
| es-ES | Spanish (Spain) | Gen CYP1A2 c.-3860G>A |
| it-IT | Italian (Italy) | CYP1A2, gene.c.-3860G>A Synonyms: Gene CYP1A2 c.-3860G>A |
| tr-TR | Turkish (Turkey) | CYP1A2 geni.c.-3860G>A |
| nl-NL | Dutch (Netherlands) | CYP1A2-gen.c.-3860G>A Synonyms: CYP1A2 gen.c.-3860G>A |
LOINC Copyright
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