Variant: rs74998556 

    present in Gene: TNFRSF13B
    present in Chromosome: 17
    Position on Chromosome: 16936468
    Alleles of this Variant: A/T

rs74998556 in TNFRSF13B gene and Monoclonal Gammopathy of Undetermined Significance PMID 30737484 2019 Genome-wide association study of monoclonal gammopathy of unknown significance (MGUS): comparison with multiple myeloma.

rs74998556 in TNFRSF13B gene and Paraproteinemias PMID 30737484 2019 Genome-wide association study of monoclonal gammopathy of unknown significance (MGUS): comparison with multiple myeloma.