Variant: rs6900762 

    present in Gene: SCGN;PRELID1P2
    present in Chromosome: 6
    Position on Chromosome: 25678816
    Alleles of this Variant: A/G

rs6900762 in SCGN;PRELID1P2 gene and Corpuscular Hemoglobin Concentration Mean PMID 23222517 2012 Seventy-five genetic loci influencing the human red blood cell.