rs10510181, CHL1-AS2

N. diseases: 4
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Adolescent idiopathic scoliosis
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
0.710 GeneticVariation BEFREE A previous genome-wide association study (GWAS) suggested a strong association between the single nucleotide polymorphism (SNP) rs10510181 in the proximity of the gene encoding a cell adhesion molecule with homology to L1CAM (CHL1) and adolescent idiopathic scoliosis (AIS) in Caucasians. 24512353 2014
Adolescent idiopathic scoliosis
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
0.710 GeneticVariation GWASDB Genome-wide association studies of adolescent idiopathic scoliosis suggest candidate susceptibility genes. 21216876 2011
SCOLIOSIS, IDIOPATHIC, SUSCEPTIBILITY TO, 1 (finding)
CUI: C2700406
Disease: SCOLIOSIS, IDIOPATHIC, SUSCEPTIBILITY TO, 1 (finding)
0.700 GeneticVariation GWASDB Genome-wide association studies of adolescent idiopathic scoliosis suggest candidate susceptibility genes. 21216876 2011
Scoliosis, unspecified
CUI: C0036439
Disease: Scoliosis, unspecified
0.700 GeneticVariation GWASCAT Genome-wide association studies of adolescent idiopathic scoliosis suggest candidate susceptibility genes. 21216876 2011
Androgen-Insensitivity Syndrome
CUI: C0039585
Disease: Androgen-Insensitivity Syndrome
0.010 GeneticVariation BEFREE Putative associations were shown between AIS and rs10510181, rs2055314, and rs2272522 in stage I. 24512353 2014