Variant: rs4844622 

    present in Gene: MIR29B2CHG
    present in Chromosome: 1
    Position on Chromosome: 207860984
    Alleles of this Variant: C/T

rs4844622 in MIR29B2CHG gene and Eosinophil count procedure PMID 27863252 2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.

rs4844622 in MIR29B2CHG gene and Granulocyte count PMID 27863252 2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.

rs4844622 in MIR29B2CHG gene and Neutrophil count (procedure) PMID 27863252 2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.

rs4844622 in MIR29B2CHG 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.