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Description

The factor II prothrombin 20210A mutation is a common genetic risk factor for thrombosis; it is associated with increased prothrombin levels. Increased prothrombin levels lead to increased thrombin generation and thus more fibrin clots. It is an autosomal dominant disorder, with heterozygotes having a 3-11 fold increased risk for thrombosis. Information from ARUP Laboratories 2007 01 08 Source: Regenstrief Institute

Basic Part Properties

Part Name
F2 gene.c.20210G>A
Part Display Name
F2 gene c.20210G>A
Part Type
Component (Describes the core component or analyte measured)
Created On
2000-05-04
Construct for LOINC Short Name
F2 c.20210G>A

LOINC Terminology Service (API) using HL7® FHIR® Get Info

CodeSystem lookup
https://fhir.loinc.org/CodeSystem/$lookup?system=http://loinc.org&code=LP14458-1
ConceptMap translate
https://fhir.loinc.org/ConceptMap/$translate?system=http://loinc.org&code=LP14458-1

Language Variants Get Info

TagLanguageTranslation
zh-CNChinese (China)F2 基因.c.20210G>A
Synonyms: F2 p.G20210A;F2 基因.p.G20210A
fr-CAFrench (Canada)Gène F2.c.20210G>A
et-EEEstonian (Estonia)F2 geen.p.G20210A
es-ESSpanish (Spain)Gen F2 polimorfismo G21210A
it-ITItalian (Italy)F2, gene.p.G20210A
Synonyms: Gene F2 p.G20210A
tr-TRTurkish (Turkey)F2 geni.p.G20210A
ru-RURussian (Russian Federation)F2 ген c.20210G>A
nl-NLDutch (Netherlands)F2-gen.c.20210G>A
Synonyms: f2 gen.c.20210G>A
fr-BEFrench (Belgium)F2 gene.c.20210G>A
fr-FRFrench (France)F2 gène mutation c.20210G>A
pl-PLPolish (Poland)F2 gen.c.20210G>A
Synonyms: Gen F2 c.20210G>A;Gen F2 c.*97G>A
el-GRGreek (Greece)Γονίδιο F2 .c.20210G>A
Synonyms: Γονίδιο F2 .c.20210G>A