Variant: rs739496 

    present in Gene: SH2B3;ATXN2
    present in Chromosome: 12
    Position on Chromosome: 111449855
    Alleles of this Variant: A/G

rs739496 in SH2B3;ATXN2 gene and Adolescent idiopathic scoliosis PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs739496 in SH2B3;ATXN2 gene and Corpuscular Hemoglobin Concentration Mean PMID 23222517 2012 Seventy-five genetic loci influencing the human red blood cell.

rs739496 in SH2B3;ATXN2 gene and Hepatitis B PMID 21750111 2011 A genome-wide association study of chronic hepatitis B identified novel risk locus in a Japanese population.

rs739496 in SH2B3;ATXN2 gene and Platelet Count measurement PMID 20139978 2010 Genome-wide association study of hematological and biochemical traits in a Japanese population.

PMID 25705162 2014 Genome-wide association study identifies candidate Loci associated with platelet count in koreans.

rs739496 in SH2B3;ATXN2 gene and Platelet mean volume determination (procedure) PMID 22423221 2012 A meta-analysis and genome-wide association study of platelet count and mean platelet volume in african americans.

rs739496 in SH2B3;ATXN2 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.