Variant: rs10172646 

    present in Gene: BCL11A
    present in Chromosome: 2
    Position on Chromosome: 60493622
    Alleles of this Variant: G/A

rs10172646 in BCL11A gene and Anemia, Sickle Cell PMID 21326311 2011 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients.

rs10172646 in BCL11A gene and Fetal hemoglobin determination PMID 17767159 2007 A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15.

PMID 18245381 2008 Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia.

PMID 21326311 2011 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients.