Variant: rs7937649 

    present in Gene: OR51V1
    present in Chromosome: 11
    Position on Chromosome: 5201149
    Alleles of this Variant: G/A;T

rs7937649 in OR51V1 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.

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