Variant: rs1003586 

    present in Gene: HBB
    present in Chromosome: 11
    Position on Chromosome: 5228140
    Alleles of this Variant: C/T

rs1003586 in HBB gene and Fetal hemoglobin determination PMID 18245381 2008 Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia.