DCC, DCC netrin 1 receptor, 1630

N. diseases: 279; N. variants: 101
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs387906555
rs387906555
Entrez Id: 1630;101928167
Gene Symbol: DCC;LINC01917
DCC;LINC01917
CUI: C0009402
Disease:
Colorectal Carcinoma 		0.800 GeneticVariation UNIPROT
dbSNP: rs4632195
rs4632195
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C0036341
Disease:
Schizophrenia 		0.710 GeneticVariation BEFREE Based on conjunctional FDR < 0.05, we identified 2 loci shared between SCZ and ICV implicating genes FOXO3 (rs10457180) and ITIH4 (rs4687658), 2 loci shared between SCZ and hippocampal volume implicating SLC4A10 (rs4664442) and SPATS2L (rs1653290), and 2 loci shared between SCZ and volume of putamen implicating DCC (rs4632195) and DLG2 (rs11233632). 29136250 2018
dbSNP: rs1039528164
rs1039528164
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C1834870
Disease:
MIRROR MOVEMENTS 1 		0.700 GeneticVariation UNIPROT
dbSNP: rs1057519056
rs1057519056
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C1834870
Disease:
MIRROR MOVEMENTS 1 		0.700 GeneticVariation UNIPROT
dbSNP: rs1057519057
rs1057519057
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C1834870
Disease:
MIRROR MOVEMENTS 1 		0.700 GeneticVariation UNIPROT
dbSNP: rs10853628
rs10853628
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C0042834
Disease:
Vital capacity 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs11082953
rs11082953
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs11082960
rs11082960
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C0153452
Disease:
Malignant neoplasm of gallbladder 		0.700 GeneticVariation GWASDB A genome-wide association study identifies SNP in DCC is associated with gallbladder cancer in the Japanese population. 22318345 2012
dbSNP: rs11663393
rs11663393
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C0525045
Disease:
Mood Disorders 		0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways. 29942085 2018
dbSNP: rs11663393
rs11663393
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C1269683
Disease:
Major Depressive Disorder 		0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways. 29942085 2018
dbSNP: rs11664123
rs11664123
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C0525045
Disease:
Mood Disorders 		0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways. 29942085 2018
dbSNP: rs11664123
rs11664123
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C1269683
Disease:
Major Depressive Disorder 		0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways. 29942085 2018
dbSNP: rs121912967
rs121912967
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C0152018
Disease:
Esophageal carcinoma 		0.700 GeneticVariation UNIPROT
dbSNP: rs1346972
rs1346972
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C0410702
Disease:
Adolescent idiopathic scoliosis 		0.700 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
dbSNP: rs1346972
rs1346972
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C1837461
Disease:
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 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
dbSNP: rs1431196
rs1431196
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C0036341
Disease:
Schizophrenia 		0.700 GeneticVariation GWASCAT Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways. 31374203 2019
dbSNP: rs1431196
rs1431196
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C0021704
Disease:
Intelligence 		0.700 GeneticVariation GWASCAT Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways. 31374203 2019
dbSNP: rs1431196
rs1431196
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C0021704
Disease:
Intelligence 		0.700 GeneticVariation GWASCAT Large-Scale Cognitive GWAS Meta-Analysis Reveals Tissue-Specific Neural Expression and Potential Nootropic Drug Targets. 29186694 2017
dbSNP: rs1555652216
rs1555652216
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C4479640
Disease:
GAZE PALSY, FAMILIAL HORIZONTAL, WITH PROGRESSIVE SCOLIOSIS, 2 		0.700 GeneticVariation UNIPROT Biallelic mutations in human DCC cause developmental split-brain syndrome. 28250456 2017
dbSNP: rs16955886
rs16955886
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C1837461
Disease:
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 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
dbSNP: rs16955886
rs16955886
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C0410702
Disease:
Adolescent idiopathic scoliosis 		0.700 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
dbSNP: rs1875560
rs1875560
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C1269683
Disease:
Major Depressive Disorder 		0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways. 29942085 2018
dbSNP: rs1875560
rs1875560
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C0525045
Disease:
Mood Disorders 		0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways. 29942085 2018
dbSNP: rs199651452
rs199651452
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C1834870
Disease:
MIRROR MOVEMENTS 1 		0.700 GeneticVariation UNIPROT
dbSNP: rs4077283
rs4077283
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C0153452
Disease:
Malignant neoplasm of gallbladder 		0.700 GeneticVariation GWASDB A genome-wide association study identifies SNP in DCC is associated with gallbladder cancer in the Japanese population. 22318345 2012