Variant: rs16978075 

    present in Gene: LINC01478;LINC01601
    present in Chromosome: 18
    Position on Chromosome: 44533186
    Alleles of this Variant: T/C

rs16978075 in LINC01478;LINC01601 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.

rs16978075 in LINC01478;LINC01601 gene and Eosinophil count procedure PMID 27863252 2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.

rs16978075 in LINC01478;LINC01601 gene and Granulocyte count PMID 27863252 2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.

rs16978075 in LINC01478;LINC01601 gene and Neutrophil count (procedure) PMID 27863252 2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.

rs16978075 in LINC01478;LINC01601 gene and mathematical ability PMID 30038396 2018 Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals.