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Article

The allele frequency of mutations in four genes that confer enhanced susceptibility to venous thromboembolism in an unselected group of New York State newborns.

Thrombosis research - 15 Aug 2000

Conroy J M, Trivedi G, Sovd T, Caggana M

Abstract excerpt

The frequencies of Factor V G1691A (FVL), prothrombin (PT) G20210A, 5'10'methylenetetrahydrofolate reductase (MTHFR) C677T, and methionine synthase (MS) A2756G (four mutations associated with an increased risk of venous thromboembolism [VTE]) were determined in a sample of approximately 1500 New York State residents. Dried blood spots from approximately equal numbers of Caucasians, African-Americans and Hispanics...

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Share to 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase
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Source

Identifiers

PMID: 10963782
DOI: 10.1016/s0049-3848(00)00254-1

Genes

MTHFR

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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