Variant: rs34891900 

    present in Gene: BCL2L13
    present in Chromosome: 22
    Position on Chromosome: 17680392
    Alleles of this Variant: C/G;T

rs34891900 in BCL2L13 gene and Eosinophil count procedure PMID 27863252 2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.

rs34891900 in BCL2L13 gene and Neutrophil count (procedure) PMID 27863252 2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.