Variant: rs17342717 

    present in Gene: SLC17A1
    present in Chromosome: 6
    Position on Chromosome: 25821542
    Alleles of this Variant: C/T

rs17342717 in SLC17A1 gene and Corpuscular Hemoglobin Concentration Mean PMID 20927387 2010 A genome-wide association study of red blood cell traits using the electronic medical record.

PMID 23222517 2012 Seventy-five genetic loci influencing the human red blood cell.

rs17342717 in SLC17A1 gene and Ferritin measurement PMID 21149283 2011 Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels.

PMID 21208937 2011 Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels.

rs17342717 in SLC17A1 gene and Finding of Mean Corpuscular Hemoglobin PMID 20927387 2010 A genome-wide association study of red blood cell traits using the electronic medical record.

PMID 22560525 2012 Genetic Loci implicated in erythroid differentiation and cell cycle regulation are associated with red blood cell traits.

rs17342717 in SLC17A1 gene and Iron level result PMID 21208937 2011 Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels.

rs17342717 in SLC17A1 gene and Iron measurement PMID 21208937 2011 Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels.

rs17342717 in SLC17A1 gene and Mean Corpuscular Volume (result) PMID 22560525 2012 Genetic Loci implicated in erythroid differentiation and cell cycle regulation are associated with red blood cell traits.

rs17342717 in SLC17A1 gene and Red Blood Cell Count measurement PMID 19862010 2009 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.

rs17342717 in SLC17A1 gene and Serum ferritin measurement PMID 21149283 2011 Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels.

PMID 21208937 2011 Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels.