Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

The 20210 A allele of the prothrombin gene is a common risk factor among Swedish outpatients with verified deep venous thrombosis.

Thrombosis and haemostasis - 1 Sept 1997

Hillarp A, Zöller B, Svensson P J, Dahlbäck B

Abstract excerpt

A dimorphism in the 3'-untranslated region of the prothrombin gene (G to A transition at position 20210) has recently been reported to be associated with increases in plasma prothrombin levels and in the risk of venous thrombosis. We have examined the prothrombin dimorphism among 99 unselected ou...

Topics

Adult
Aged
Aged, 80 and over
Alleles
Female
Gene Frequency
Humans
Male
Middle Aged
Outpatients
Phlebography
Protein C
Prothrombin

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Risk Factors

Sweden

Thrombophlebitis

Source

Identifiers

PMID: 9308741

Genes

APC

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-9308741-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The 20210 A allele of the prothrombin gene is a common risk factor among Swedish outpatients with verified deep venous thrombosis.PMID 9308741Read ↗

A common genetic variation in the 3'-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis.Semantic proximity Read ↗

The prothrombin 20210 G to A variation and thrombosis.Semantic proximity Read ↗

The prothrombin 20210A allele is the most prevalent genetic risk factor for venous thromboembolism in the Spanish population.Semantic proximity Read ↗

Prevalence of 20210 A allele of the prothrombin gene in venous thromboembolism patients.Semantic proximity Read ↗

Prevalence of the prothrombin gene variant (nt20210A) in venous thrombosis and arterial disease.Semantic proximity Read ↗

The prothrombin gene variant 20210A in venous and arterial thromboembolism.Semantic proximity Read ↗

The heterozygous 20210 G/A prothrombin genotype is associated with early venous thrombosis in inherited thrombophilias and is not increased in frequency in artery disease.Semantic proximity Read ↗

[20210A mutation of the prothrombin and venous thromboembolism gene].Semantic proximity Read ↗

The 20210 G → A mutation in the 3′‐untranslated region of the prothrombin gene and the risk for arterial thrombotic diseaseSemantic proximity Read ↗

The prothrombin nt20210 A allele as a risk factor for venous thromboembolism: detection of heterozygous and homozygous carriers by alternative methods.Semantic proximity Read ↗

Homozygotes for prothrombin gene 20210 A allele in a thrombophilic family without clinical manifestations of venous thromboembolism.Semantic proximity Read ↗

Prevalence of the G20210A polymorphism in the 3'-untranslated region of the prothrombin gene in different human populations.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.