Variant: rs121913088 

    present in Gene: FGG
    present in Chromosome: 4
    Position on Chromosome: 154606932
    Alleles of this Variant: C/T

rs121913088 in FGG gene and Dysfibrinogenemia, Congenital PMID 2257302 1990 Fibrinogen Baltimore I: polymerization defect associated with a gamma 292Gly----Val (GGC----GTC) mutation.

PMID 2976995 1988 "Normal plasmic cleavage of the gamma-chain variant of ""fibrinogen Saga"" with an Arg-275 to His substitution."

PMID 3708159 1986 Characterization of fibrinogen Milano I: amino acid exchange gamma 330 Asp----Val impairs fibrin polymerization.

PMID 15632207 2005 Fibrinogen Philadelphia, a hypodysfibrinogenemia characterized by abnormal polymerization and fibrinogen hypercatabolism due to gamma S378P mutation.

rs121913088 in FGG gene and Hypofibrinogenemia PMID 31064749 2019 Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders.