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Article

The prothrombin gene G20210A variant: prevalence in a U.K. anticoagulant clinic population

1 Aug 1997

Abstract excerpt

We have investigated the prevalence of a recently reported genetic variation in the prothrombin gene (G20210A) in patients with an objectively confirmed history of venous thrombosis, 12/219 patients (5.5%) were found to be heterozygous carriers of the 20210A allele. The incidence of the 20210A allele in a group of 164 healthy controls was 1.2% (allele frequency 0.61%, 95% CI 0.08-2.19). When patients with a known...

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Identifiers

PMID: 9266933
DOI: 10.1046/j.1365-2141.1997.2353052.x

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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The prothrombin gene G20210A variant: prevalence in a U.K. anticoagulant clinic populationPMID 9266933Read ↗

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