Source: GWASCAT

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 57537
Gene Symbol: SORCS2
SORCS2
CUI: C0236663
Disease: Alcohol withdrawal syndrome
Alcohol withdrawal syndrome 		0.120 GeneticVariation GWASCAT Risk Locus Identification Ties Alcohol Withdrawal Symptoms to SORCS2. 30252935

2018
Entrez Id: 57537
Gene Symbol: SORCS2
SORCS2
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		0.100 GeneticVariation 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: 57537
Gene Symbol: SORCS2
SORCS2
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.100 GeneticVariation 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: 57537
Gene Symbol: SORCS2
SORCS2
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.100 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488

2018
Entrez Id: 57537
Gene Symbol: SORCS2
SORCS2
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.100 GeneticVariation GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576

2018
Entrez Id: 57537
Gene Symbol: SORCS2
SORCS2
CUI: C0002895
Disease: Anemia, Sickle Cell
Anemia, Sickle Cell 		0.100 GeneticVariation GWASCAT Genome-wide association study of erythrocyte density in sickle cell disease patients. 28552477

2017
Entrez Id: 57537
Gene Symbol: SORCS2
SORCS2
CUI: C0003125
Disease: Anorexia Nervosa
Anorexia Nervosa 		0.100 GeneticVariation GWASCAT Significant Locus and Metabolic Genetic Correlations Revealed in Genome-Wide Association Study of Anorexia Nervosa. 28494655

2017
Entrez Id: 57537
Gene Symbol: SORCS2
SORCS2
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.100 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959

2017
Entrez Id: 57537
Gene Symbol: SORCS2
SORCS2
CUI: C1277709
Disease: Transferrin saturation measurement
Transferrin saturation measurement 		0.100 GeneticVariation GWASCAT Genome-wide association study of iron traits and relation to diabetes in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL): potential genomic intersection of iron and glucose regulation? 28334935

2017
Entrez Id: 57537
Gene Symbol: SORCS2
SORCS2
CUI: C2697758
Disease: Interleukin 10 Measurement
Interleukin 10 Measurement 		0.100 GeneticVariation GWASCAT Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors. 27989323

2017
Entrez Id: 57537
Gene Symbol: SORCS2
SORCS2
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		0.100 GeneticVariation GWASCAT New suggestive genetic loci and biological pathways for attention function in adult attention-deficit/hyperactivity disorder. 26174813

2015