rs10226084 - SNX13 - MRM3P2
Magnitude 2.2 · 1 study on file
Reported associations
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A Multi-Ethnic Meta-Analysis of Genome-Wide Association Studies in Over 100,000 Subjects Identifies 23 Fibrinogen-Associated Loci but no Strong Evidence of a Causal Association between Circulating Fibrinogen and Cardiovascular Disease - Unknown journal (n.d.) · Unknown authors · PubMed 23969696
ABSTRACT: Background Estimates of the heritability of plasma fibrinogen concentration, an established predictor of cardiovascular disease (CVD), range from 34 to 50%. Genetic variants so far identified by genome-wide association (GWA) studies only explain a small proportion (< 2%) of its variation. Methods and Results We conducted a meta-analysis of 28 GWA studies, including more than 90,000 subjects of European ancestry, the first GWA meta-analysis of fibrinogen levels in 7 African Americans studies totaling 8,289 samples, and a GWA study in Hispanic-Americans totaling 1,366 samples. Evaluation for association of SNPs with clinical outcomes included a total of 40,695 cases and 85,582 controls for coronary artery disease (CAD), 4,752 cases and 24,030 controls for stroke, and 3,208 cases an
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Lifestyle context
Concrete actions anchored to the cited research. We do not prescribe, we describe.
Screening
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Fibrinogen level Moderate
rs10226084 is associated with fibrinogen levels (p=5e-10), a coagulation factor affecting cardiovascular thrombotic risk.
Obtain baseline fibrinogen measurement; monitor per clinical guidelines