Variant: rs121913087 

    present in Gene: FGG
    present in Chromosome: 4
    Position on Chromosome: 154606933
    Alleles of this Variant: G/A

rs121913087 in FGG gene and Hypofibrinogenemia PMID 31064749 2019 Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders.