DCX, doublecortin, 1641

N. diseases: 175; N. variants: 107
Disease: Lissencephaly and agenesis of corpus callosum ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894779
rs104894779
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C1848070
Disease:
Lissencephaly and agenesis of corpus callosum 		T 0.700 CausalMutation CLINVAR
dbSNP: rs104894780
rs104894780
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C1848070
Disease:
Lissencephaly and agenesis of corpus callosum 		A 0.700 CausalMutation CLINVAR
dbSNP: rs104894781
rs104894781
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C1848070
Disease:
Lissencephaly and agenesis of corpus callosum 		G 0.700 CausalMutation CLINVAR
dbSNP: rs104894782
rs104894782
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C1848070
Disease:
Lissencephaly and agenesis of corpus callosum 		C 0.700 CausalMutation CLINVAR
dbSNP: rs104894783
rs104894783
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C1848070
Disease:
Lissencephaly and agenesis of corpus callosum 		G 0.700 CausalMutation CLINVAR
dbSNP: rs104894786
rs104894786
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C1848070
Disease:
Lissencephaly and agenesis of corpus callosum 		A 0.700 CausalMutation CLINVAR
dbSNP: rs122457137
rs122457137
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C1848070
Disease:
Lissencephaly and agenesis of corpus callosum 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1556401725
rs1556401725
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C1848070
Disease:
Lissencephaly and agenesis of corpus callosum 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1556401744
rs1556401744
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C1848070
Disease:
Lissencephaly and agenesis of corpus callosum 		T 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: rs56030372
rs56030372
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C1848070
Disease:
Lissencephaly and agenesis of corpus callosum 		T 0.700 CausalMutation CLINVAR