Variant: rs7875291 

    present in Gene: LOC101929507
    present in Chromosome: 9
    Position on Chromosome: 13980153
    Alleles of this Variant: G/A

rs7875291 in LOC101929507 gene and Hematocrit procedure PMID 27863252 2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.

rs7875291 in LOC101929507 gene and Hemoglobin measurement PMID 27863252 2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.

rs7875291 in LOC101929507 gene and Red Blood Cell Count measurement PMID 27863252 2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.