Variant: rs200748895 

    present in Gene: TNFSF13B
    present in Chromosome: 13
    Position on Chromosome: 108308033
    Alleles of this Variant: GCTG/-

rs200748895 in TNFSF13B gene and Platelet Count measurement PMID 27863252 2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.

rs200748895 in TNFSF13B gene and White Blood Cell Count procedure PMID 27863252 2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.