Variant: rs4910742 

    present in Gene: HBG2;HBE1
    present in Chromosome: 11
    Position on Chromosome: 5285279
    Alleles of this Variant: G/A;T

rs4910742 in HBG2;HBE1 gene and Blood Sedimentation PMID 22291609 2012 A genome-wide association scan on the levels of markers of inflammation in Sardinians reveals associations that underpin its complex regulation.

rs4910742 in HBG2;HBE1 gene and C-reactive protein measurement PMID 22291609 2012 A genome-wide association scan on the levels of markers of inflammation in Sardinians reveals associations that underpin its complex regulation.

rs4910742 in HBG2;HBE1 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.