Variant: rs1003688 

    present in Gene: SCGN
    present in Chromosome: 6
    Position on Chromosome: 25658944
    Alleles of this Variant: G/A

rs1003688 in SCGN gene and Corpuscular Hemoglobin Concentration Mean PMID 23222517 2012 Seventy-five genetic loci influencing the human red blood cell.

rs1003688 in SCGN gene and Red Blood Cell Count measurement PMID 19862010 2009 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.