Variant: rs121909616 

    present in Gene: FGB
    present in Chromosome: 4
    Position on Chromosome: 154565823
    Alleles of this Variant: C/T

rs121909616 in FGB gene and Hypofibrinogenemia PMID 31064749 2019 Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders.