Variant: rs121909606 

    present in Gene: FGA
    present in Chromosome: 4
    Position on Chromosome: 154589514
    Alleles of this Variant: G/A

rs121909606 in FGA gene and Dysfibrinogenemia, Congenital PMID 8473507 1993 Molecular basis for fibrinogen Dusart (A alpha 554 Arg-->Cys) and its association with abnormal fibrin polymerization and thrombophilia.

PMID 16846481 2006 The fibrinogen Aalpha R16C mutation results in fibrinolytic resistance.