Variant: rs10489629 

    present in Gene: IL23R;C1orf141
    present in Chromosome: 1
    Position on Chromosome: 67222666
    Alleles of this Variant: T/C

rs10489629 in IL23R;C1orf141 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.

rs10489629 in IL23R;C1orf141 gene and Crohn Disease PMID 17068223 2006 A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.

rs10489629 in IL23R;C1orf141 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.