LP14458-1
F2 gene.c.20210G>A
Active
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 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
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Language Variants Get Info
| Tag | Language | Translation |
|---|---|---|
| zh-CN | Chinese (China) | F2 基因.c.20210G>A Synonyms: F2 p.G20210A; |
| fr-CA | French (Canada) | Gène F2.c.20210G>A |
| et-EE | Estonian (Estonia) | F2 geen.p.G20210A |
| es-ES | Spanish (Spain) | Gen F2 polimorfismo G21210A |
| it-IT | Italian (Italy) | F2, gene.p.G20210A Synonyms: Gene F2 p.G20210A |
| tr-TR | Turkish (Turkey) | F2 geni.p.G20210A |
| ru-RU | Russian (Russian Federation) | F2 ген c.20210G>A |
| nl-NL | Dutch (Netherlands) | F2-gen.c.20210G>A Synonyms: f2 gen.c.20210G>A |
| fr-BE | French (Belgium) | F2 gene.c.20210G>A |
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