Variant: rs75848804 

    present in Gene: FGG
    present in Chromosome: 4
    Position on Chromosome: 154604995
    Alleles of this Variant: G/A;C;T

rs75848804 in FGG gene and Congenital hypofibrinogenemia PMID 25427968 2015 Clinical and molecular characterisation of 21 patients affected by quantitative fibrinogen deficiency.