Variant: rs2208568 

    present in Gene: LOC105373215;LINC02768
    present in Chromosome: 1
    Position on Chromosome: 235926855
    Alleles of this Variant: T/A;C;G

rs2208568 in LOC105373215;LINC02768 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.

rs2208568 in LOC105373215;LINC02768 gene and Eosinophil count procedure PMID 27863252 2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.

rs2208568 in LOC105373215;LINC02768 gene and Granulocyte count PMID 27863252 2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.

rs2208568 in LOC105373215;LINC02768 gene and Neutrophil count (procedure) PMID 27863252 2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.

rs2208568 in LOC105373215;LINC02768 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.