Variant: rs10768980 

    present in Gene: HBG2;HBE1;OR51B5
    present in Chromosome: 11
    Position on Chromosome: 5470803
    Alleles of this Variant: C/G

rs10768980 in HBG2;HBE1;OR51B5 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.