10q23 g.94645745G A:Geno:Pt:Bld/Tiss:Nom:Molgen

Preferred Label : 10q23 g.94645745G A:Geno:Pt:Bld/Tiss:Nom:Molgen;

LOINC status : ACTIVE;

LOINC display name : 10q23 g.94645745G A genotype Molgen (Bld/Tiss);

LOINC long common name : 10q23 g.94645745G A [Genotype] in Blood or Tissue by Molecular genetics method Nominal;

LOINC short name : 10q23 g.94645745G A Geno Bld/T;

LOINC description : The non-coding variant g.94645745G A (rs12777823) located in the CYP2C cluster near the CYP2C18 gene on chromosome 10 is associated with warfarin dosing among African Americans (mainly originating from West Africa). For those with rs12777823 A/G or A/A genotypes, a warfarin dose reduction of 10-25% is recommended.[PMID: 28198005];

Details

Origin ID

93198-0;

UMLS CUI

C5211636;

Has component
- 10q23 g.94645745G>A [LOINC component]
Has method
- Molecular genetics [LOINC method]
Has property
- Genotype [LOINC Property]
Has scale
- Nom [LOINC scale]
Has system
- Blood [LOINC System]
- Blood or Tissue [LOINC System]
- Tissue and Smears [LOINC System]
Has time aspect
- Point in time (spot) [LOINC time aspect]
Part of panel
- Warfarin response genotype panel:-:Pt:Bld/Tiss:-:Molgen [LOINC code]
Semantic type(s)
- Clinical Attribute [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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