Variant: rs1800787 

    present in Gene: FGB
    present in Chromosome: 4
    Position on Chromosome: 154562863
    Alleles of this Variant: C/T

rs1800787 in FGB gene and Fibrinogen assay PMID 20978265 2011 Common fibrinogen gene single nucleotide polymorphisms (FGB rs1800787 and FGG rs2066861) significantly associated with fibrinogen in EAs were prevalent in AAs and showed consistent associations.

rs1800787 in FGB gene and Fibrinogen, CTCAE PMID 20978265 2011 Common fibrinogen gene single nucleotide polymorphisms (FGB rs1800787 and FGG rs2066861) significantly associated with fibrinogen in EAs were prevalent in AAs and showed consistent associations.

rs1800787 in FGB gene and fibrinogen activity PMID 20978265 2011 Common fibrinogen gene single nucleotide polymorphisms (FGB rs1800787 and FGG rs2066861) significantly associated with fibrinogen in EAs were prevalent in AAs and showed consistent associations.