Variant: rs6054 

    present in Gene: FGB
    present in Chromosome: 4
    Position on Chromosome: 154568456
    Alleles of this Variant: C/T

rs6054 in FGB gene and Bleeding tendency PMID 31064749 2019 Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders.

rs6054 in FGB gene and Fibrinogen assay PMID 20978265 2011 We identified a rare Pro265Leu variant in FGB (rs6054) associated with lower fibrinogen.

PMID 26561523 2016 A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration.

rs6054 in FGB gene and Fibrinogen, CTCAE PMID 20978265 2011 We identified a rare Pro265Leu variant in FGB (rs6054) associated with lower fibrinogen.

rs6054 in FGB gene and Serum total cholesterol measurement PMID 29083408 2017 Exome-wide association study of plasma lipids in >300,000 individuals.

rs6054 in FGB gene and fibrinogen activity PMID 20978265 2011 We identified a rare Pro265Leu variant in FGB (rs6054) associated with lower fibrinogen.