Variant: rs7745098

present in Gene: HBS1L present in Chromosome: 6 Position on Chromosome: 135093866 Alleles of this Variant: C/G;T

rs7745098 in HBS1L gene and Corpuscular Hemoglobin Concentration Mean PMID 23222517 2012 Seventy-five genetic loci influencing the human red blood cell.

rs7745098 in HBS1L gene and Hodgkin Disease PMID 24149102 2013 A combined analysis identifies new HL susceptibility loci mapping to 3p24.1 (rs3806624; P=1.14 × 10(-12), odds ratio (OR)=1.26) and 6q23.3 (rs7745098; P=3.42 × 10(-9), OR=1.21). rs3806624 localizes 5' to the EOMES (eomesodermin) gene within a p53 response element affecting p53 binding. rs7745098 maps intergenic to HBS1L and MYB, a region previously associated with haematopoiesis.