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: 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: rs4632195
rs4632195
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C0036341
Disease:
Schizophrenia 		T 0.710 GeneticVariation GWASCAT Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect. 30285260 2019
dbSNP: rs10221412
rs10221412
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C0021704
Disease:
Intelligence 		T 0.700 GeneticVariation GWASCAT A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence. 29326435 2019
dbSNP: rs1039528164
rs1039528164
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C1834870
Disease:
MIRROR MOVEMENTS 1 		0.700 GeneticVariation UNIPROT
dbSNP: rs10502966
rs10502966
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C0021704
Disease:
Intelligence 		A 0.700 GeneticVariation GWASCAT A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence. 29326435 2019
dbSNP: rs1057519053
rs1057519053
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C0175754
Disease:
Agenesis of corpus callosum 		T 0.700 CausalMutation CLINVAR
dbSNP: rs1057519053
rs1057519053
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C1834870
Disease:
MIRROR MOVEMENTS 1 		T 0.700 CausalMutation CLINVAR
dbSNP: rs1057519054
rs1057519054
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C1834870
Disease:
MIRROR MOVEMENTS 1 		G 0.700 CausalMutation CLINVAR
dbSNP: rs1057519054
rs1057519054
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C0175754
Disease:
Agenesis of corpus callosum 		G 0.700 CausalMutation CLINVAR
dbSNP: rs1057519055
rs1057519055
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C0175754
Disease:
Agenesis of corpus callosum 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1057519055
rs1057519055
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C1834870
Disease:
MIRROR MOVEMENTS 1 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1057519056
rs1057519056
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C0175754
Disease:
Agenesis of corpus callosum 		C 0.700 CausalMutation CLINVAR
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: C0175754
Disease:
Agenesis of corpus callosum 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1057519057
rs1057519057
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C1834870
Disease:
MIRROR MOVEMENTS 1 		0.700 GeneticVariation UNIPROT
dbSNP: rs1078459
rs1078459
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C0021704
Disease:
Intelligence 		T 0.700 GeneticVariation GWASCAT Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. 29942086 2018
dbSNP: rs1078459
rs1078459
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C0021704
Disease:
Intelligence 		T 0.700 GeneticVariation GWASCAT A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence. 29326435 2019
dbSNP: rs10853627
rs10853627
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C0021704
Disease:
Intelligence 		T 0.700 GeneticVariation GWASCAT Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. 29942086 2018
dbSNP: rs10853627
rs10853627
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C0021704
Disease:
Intelligence 		T 0.700 GeneticVariation GWASCAT Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. 29844566 2018
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: rs11662271
rs11662271
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C0021704
Disease:
Intelligence 		T 0.700 GeneticVariation GWASCAT Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. 29844566 2018
dbSNP: rs11663156
rs11663156
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C0021704
Disease:
Intelligence 		T 0.700 GeneticVariation GWASCAT Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. 29942086 2018
dbSNP: rs11663156
rs11663156
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C0021704
Disease:
Intelligence 		T 0.700 GeneticVariation GWASCAT A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence. 29326435 2019