Variant: rs10075801 

    present in Gene: MIR3936HG;SLC22A4
    present in Chromosome: 5
    Position on Chromosome: 132341949
    Alleles of this Variant: A/G

rs10075801 in MIR3936HG;SLC22A4 gene and Blood basophil count (lab test) PMID 27863252 2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.

rs10075801 in MIR3936HG;SLC22A4 gene and Eosinophil count procedure PMID 27863252 2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.

rs10075801 in MIR3936HG;SLC22A4 gene and Granulocyte count PMID 27863252 2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.

rs10075801 in MIR3936HG;SLC22A4 gene and Neutrophil count (procedure) PMID 27863252 2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.

rs10075801 in MIR3936HG;SLC22A4 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.