Variant: rs7148590 

    present in Gene: CHURC1-FNTB;FNTB;MAX
    present in Chromosome: 14
    Position on Chromosome: 65006478
    Alleles of this Variant: G/A

rs7148590 in CHURC1-FNTB;FNTB;MAX gene and Corpuscular Hemoglobin Concentration Mean PMID 23222517 2012 Seventy-five genetic loci influencing the human red blood cell.

rs7148590 in CHURC1-FNTB;FNTB;MAX gene and Red Blood Cell Count measurement PMID 19862010 2009 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.

rs7148590 in CHURC1-FNTB;FNTB;MAX gene and Serum zinc measurement PMID 23720494 2013 Genome-wide association study identifies loci affecting blood copper, selenium and zinc.