DCX, doublecortin, 1641

N. diseases: 175; N. variants: 107
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1556401744
rs1556401744
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1
T 0.700 CausalMutation CLINVAR
dbSNP: rs1556401951
rs1556401951
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1
A 0.700 CausalMutation CLINVAR
dbSNP: rs1556404991
rs1556404991
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C1848070
Disease:
Lissencephaly and agenesis of corpus callosum
C 0.700 CausalMutation CLINVAR
dbSNP: rs1556405057
rs1556405057
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C0016788
Disease:
Fucosidase Deficiency Disease
T 0.700 CausalMutation CLINVAR
dbSNP: rs1556405129
rs1556405129
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1
T 0.700 GeneticVariation CLINVAR Comprehensive genomic analysis of patients with disorders of cerebral cortical development. 29706646 2018
dbSNP: rs1556405129
rs1556405129
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C1837249
Disease:
Malformations of Cortical Development, Group II
T 0.700 GeneticVariation CLINVAR Comprehensive genomic analysis of patients with disorders of cerebral cortical development. 29706646 2018
dbSNP: rs1569497266
rs1569497266
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1
C 0.700 CausalMutation CLINVAR
dbSNP: rs1569498597
rs1569498597
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1
ATC 0.700 CausalMutation CLINVAR
dbSNP: rs201870761
rs201870761
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C1837249
Disease:
Malformations of Cortical Development, Group II
A 0.700 CausalMutation CLINVAR
dbSNP: rs267606317
rs267606317
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C1837249
Disease:
Malformations of Cortical Development, Group II
T 0.700 CausalMutation CLINVAR
dbSNP: rs56030372
rs56030372
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C1837249
Disease:
Malformations of Cortical Development, Group II
T 0.700 CausalMutation CLINVAR
dbSNP: rs56030372
rs56030372
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C1848070
Disease:
Lissencephaly and agenesis of corpus callosum
T 0.700 CausalMutation CLINVAR
dbSNP: rs587783518
rs587783518
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C1837249
Disease:
Malformations of Cortical Development, Group II
C 0.700 CausalMutation CLINVAR
dbSNP: rs587783519
rs587783519
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C1837249
Disease:
Malformations of Cortical Development, Group II
A 0.700 CausalMutation CLINVAR
dbSNP: rs587783520
rs587783520
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C1837249
Disease:
Malformations of Cortical Development, Group II
G 0.700 CausalMutation CLINVAR
dbSNP: rs587783521
rs587783521
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C1837249
Disease:
Malformations of Cortical Development, Group II
G 0.700 CausalMutation CLINVAR
dbSNP: rs587783522
rs587783522
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C1837249
Disease:
Malformations of Cortical Development, Group II
A 0.700 CausalMutation CLINVAR
dbSNP: rs587783523
rs587783523
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C1837249
Disease:
Malformations of Cortical Development, Group II
A 0.700 CausalMutation CLINVAR
dbSNP: rs587783524
rs587783524
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C1837249
Disease:
Malformations of Cortical Development, Group II
G 0.700 CausalMutation CLINVAR
dbSNP: rs587783525
rs587783525
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C1837249
Disease:
Malformations of Cortical Development, Group II
G 0.700 GeneticVariation CLINVAR
dbSNP: rs587783526
rs587783526
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C1837249
Disease:
Malformations of Cortical Development, Group II
C 0.700 GeneticVariation CLINVAR
dbSNP: rs587783527
rs587783527
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C1837249
Disease:
Malformations of Cortical Development, Group II
T 0.700 CausalMutation CLINVAR
dbSNP: rs587783528
rs587783528
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C1837249
Disease:
Malformations of Cortical Development, Group II
C 0.700 GeneticVariation CLINVAR
dbSNP: rs587783529
rs587783529
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C1837249
Disease:
Malformations of Cortical Development, Group II
A 0.700 GeneticVariation CLINVAR
dbSNP: rs587783530
rs587783530
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C1837249
Disease:
Malformations of Cortical Development, Group II
C 0.700 GeneticVariation CLINVAR