Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 55636
Gene Symbol: CHD7
CHD7
0.400 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 54796
Gene Symbol: BNC2
BNC2
0.100 GeneticVariation disease GWASCAT A Functional SNP in BNC2 Is Associated with Adolescent Idiopathic Scoliosis. 26211971 2015
Entrez Id: 596
Gene Symbol: BCL2
BCL2
0.100 GeneticVariation disease GWASCAT Genome-wide association study identifies new susceptibility loci for adolescent idiopathic scoliosis in Chinese girls. 26394188 2015
Entrez Id: 399806
Gene Symbol: LBX1-AS1
LBX1-AS1
0.100 GeneticVariation disease GWASCAT Genome-wide association study identifies new susceptibility loci for adolescent idiopathic scoliosis in Chinese girls. 26394188 2015
Entrez Id: 23043
Gene Symbol: TNIK
TNIK
0.100 GeneticVariation disease GWASCAT Genome-wide association study identifies novel susceptible loci and highlights Wnt/beta-catenin pathway in the development of adolescent idiopathic scoliosis. 28334814 2017
Entrez Id: 9223
Gene Symbol: MAGI1
MAGI1
0.100 GeneticVariation disease GWASCAT Genome-wide association study identifies novel susceptible loci and highlights Wnt/beta-catenin pathway in the development of adolescent idiopathic scoliosis. 28334814 2017
Entrez Id: 399806
Gene Symbol: LBX1-AS1
LBX1-AS1
0.100 GeneticVariation disease GWASCAT Genome-wide association study identifies novel susceptible loci and highlights Wnt/beta-catenin pathway in the development of adolescent idiopathic scoliosis. 28334814 2017
Entrez Id: 100507073
Gene Symbol: LINC01798
LINC01798
0.100 GeneticVariation disease GWASCAT Genome-wide association study identifies novel susceptible loci and highlights Wnt/beta-catenin pathway in the development of adolescent idiopathic scoliosis. 28334814 2017
Entrez Id: 596
Gene Symbol: BCL2
BCL2
0.100 GeneticVariation disease GWASCAT Genome-wide association study identifies novel susceptible loci and highlights Wnt/beta-catenin pathway in the development of adolescent idiopathic scoliosis. 28334814 2017
Entrez Id: 101928989
Gene Symbol: MIR4300HG
MIR4300HG
0.100 GeneticVariation disease GWASCAT A functional variant in MIR4300HG, the host gene of microRNA MIR4300 is associated with progression of adolescent idiopathic scoliosis. 29016859 2017
Entrez Id: 55636
Gene Symbol: CHD7
CHD7
0.400 GeneticVariation disease GWASCAT 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. 30019117 2018
Entrez Id: 105463123
Gene Symbol: XACT
XACT
0.100 GeneticVariation disease GWASCAT 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. 30019117 2018
Entrez Id: 100874058
Gene Symbol: COX10-AS1
COX10-AS1
0.100 GeneticVariation disease GWASCAT 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. 30019117 2018
Entrez Id: 347516
Gene Symbol: DGAT2L6
DGAT2L6
0.100 GeneticVariation disease GWASCAT 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. 30019117 2018
Entrez Id: 9317
Gene Symbol: PTER
PTER
0.100 GeneticVariation disease GWASCAT 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. 30019117 2018
Entrez Id: 7528
Gene Symbol: YY1
YY1
0.100 GeneticVariation disease GWASCAT 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. 30019117 2018
Entrez Id: 57787
Gene Symbol: MARK4
MARK4
0.100 GeneticVariation disease GWASCAT 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. 30019117 2018
Entrez Id: 23281
Gene Symbol: MTUS2
MTUS2
0.100 GeneticVariation disease GWASCAT 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. 30019117 2018
Entrez Id: 101927891
Gene Symbol: PKN2-AS1
PKN2-AS1
0.100 GeneticVariation disease GWASCAT 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. 30019117 2018
Entrez Id: 5362
Gene Symbol: PLXNA2
PLXNA2
0.100 GeneticVariation disease GWASCAT 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. 30019117 2018
Entrez Id: 253430
Gene Symbol: IPMK
IPMK
0.100 GeneticVariation disease GWASCAT 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. 30019117 2018
Entrez Id: 10666
Gene Symbol: CD226
CD226
0.100 GeneticVariation disease GWASCAT 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. 30019117 2018
Entrez Id: 100048912
Gene Symbol: CDKN2B-AS1
CDKN2B-AS1
0.100 GeneticVariation disease GWASCAT 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. 30019117 2018
Entrez Id: 79698
Gene Symbol: ZMAT4
ZMAT4
0.100 GeneticVariation disease GWASCAT 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. 30019117 2018
Entrez Id: 57580
Gene Symbol: PREX1
PREX1
0.100 GeneticVariation disease GWASCAT 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. 30019117 2018