rs5974155 in
XACT 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.
rs5929166 in
XACT gene and
Crohn Disease
PMID 28067912 2017 Genome-wide association study identifies distinct genetic contributions to prognosis and susceptibility in Crohn's disease.
rs5974155 in
XACT 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.