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: rs387906555
rs387906555
Entrez Id: 1630;101928167
Gene Symbol: DCC;LINC01917
DCC;LINC01917
CUI: C0009402
Disease:
Colorectal Carcinoma
A 0.800 CausalMutation CLINVAR
dbSNP: rs1039528164
rs1039528164
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C1834870
Disease:
MIRROR MOVEMENTS 1
0.700 GeneticVariation UNIPROT
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: rs121912967
rs121912967
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C0152018
Disease:
Esophageal carcinoma
0.700 GeneticVariation UNIPROT
dbSNP: rs121912967
rs121912967
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C4015970
Disease:
ESOPHAGEAL CARCINOMA, SOMATIC
C 0.700 CausalMutation CLINVAR
dbSNP: rs1568364038
rs1568364038
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C1855710
Disease:
Bone marrow hypocellularity
C 0.700 GeneticVariation CLINVAR
dbSNP: rs199651452
rs199651452
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C1834870
Disease:
MIRROR MOVEMENTS 1
0.700 GeneticVariation UNIPROT
dbSNP: rs199651452
rs199651452
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C0175754
Disease:
Agenesis of corpus callosum
T 0.700 CausalMutation CLINVAR
dbSNP: rs748112308
rs748112308
Entrez Id: 1630;101928167
Gene Symbol: DCC;LINC01917
DCC;LINC01917
CUI: C1834870
Disease:
MIRROR MOVEMENTS 1
0.700 GeneticVariation UNIPROT
dbSNP: rs754914260
rs754914260
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C0175754
Disease:
Agenesis of corpus callosum
T 0.700 CausalMutation CLINVAR
dbSNP: rs754914260
rs754914260
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C1834870
Disease:
MIRROR MOVEMENTS 1
T 0.700 CausalMutation CLINVAR
dbSNP: rs775565634
rs775565634
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C0175754
Disease:
Agenesis of corpus callosum
A 0.700 CausalMutation CLINVAR
dbSNP: rs775565634
rs775565634
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C1834870
Disease:
MIRROR MOVEMENTS 1
0.700 GeneticVariation UNIPROT
dbSNP: rs797044556
rs797044556
Entrez Id: 1630;101928167
Gene Symbol: DCC;LINC01917
DCC;LINC01917
CUI: C1834870
Disease:
MIRROR MOVEMENTS 1
A 0.700 CausalMutation CLINVAR
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