RS2066861 Unknown gene

Other Chr 4:154606284
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What This Variant Does
"Association of genomic loci from a cardiovascular gene SNP array with fibrinogen levels in European Americans and African-Americans from six cohort studies: the Candidate gene Association Resource (CARe)"
GWAS Studies (2)
Trait Risk Allele OR / Beta P-value Study
Prothrombin time β: 0.054 2E-20 PubMed
Coagulation defects (PheCode 286) C OR: 0.11 2E-16 PubMed
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