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: rs104894779
rs104894779
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT A novel DCX missense mutation in a family with X-linked lissencephaly and subcortical band heterotopia syndrome inherited from a low-level somatic mosaic mother: Genetic and functional studies. 27292316 2016
dbSNP: rs104894780
rs104894780
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT A novel DCX missense mutation in a family with X-linked lissencephaly and subcortical band heterotopia syndrome inherited from a low-level somatic mosaic mother: Genetic and functional studies. 27292316 2016
dbSNP: rs104894781
rs104894781
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT A novel DCX missense mutation in a family with X-linked lissencephaly and subcortical band heterotopia syndrome inherited from a low-level somatic mosaic mother: Genetic and functional studies. 27292316 2016
dbSNP: rs104894782
rs104894782
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT A novel DCX missense mutation in a family with X-linked lissencephaly and subcortical band heterotopia syndrome inherited from a low-level somatic mosaic mother: Genetic and functional studies. 27292316 2016
dbSNP: rs104894783
rs104894783
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT A novel DCX missense mutation in a family with X-linked lissencephaly and subcortical band heterotopia syndrome inherited from a low-level somatic mosaic mother: Genetic and functional studies. 27292316 2016
dbSNP: rs104894786
rs104894786
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT A novel DCX missense mutation in a family with X-linked lissencephaly and subcortical band heterotopia syndrome inherited from a low-level somatic mosaic mother: Genetic and functional studies. 27292316 2016
dbSNP: rs122457137
rs122457137
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT A novel DCX missense mutation in a family with X-linked lissencephaly and subcortical band heterotopia syndrome inherited from a low-level somatic mosaic mother: Genetic and functional studies. 27292316 2016
dbSNP: rs56030372
rs56030372
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT A novel DCX missense mutation in a family with X-linked lissencephaly and subcortical band heterotopia syndrome inherited from a low-level somatic mosaic mother: Genetic and functional studies. 27292316 2016
dbSNP: rs104894779
rs104894779
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT Somatic mosaicism and variable penetrance in doublecortin-associated migration disorders. 12552055 2003
dbSNP: rs104894780
rs104894780
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT Somatic mosaicism and variable penetrance in doublecortin-associated migration disorders. 12552055 2003
dbSNP: rs104894781
rs104894781
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT Somatic mosaicism and variable penetrance in doublecortin-associated migration disorders. 12552055 2003
dbSNP: rs104894782
rs104894782
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT Somatic mosaicism and variable penetrance in doublecortin-associated migration disorders. 12552055 2003
dbSNP: rs104894783
rs104894783
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT Somatic mosaicism and variable penetrance in doublecortin-associated migration disorders. 12552055 2003
dbSNP: rs104894786
rs104894786
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT Somatic mosaicism and variable penetrance in doublecortin-associated migration disorders. 12552055 2003
dbSNP: rs122457137
rs122457137
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT Somatic mosaicism and variable penetrance in doublecortin-associated migration disorders. 12552055 2003
dbSNP: rs56030372
rs56030372
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT Somatic mosaicism and variable penetrance in doublecortin-associated migration disorders. 12552055 2003
dbSNP: rs104894779
rs104894779
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT Subcortical band heterotopia (SBH) in males: clinical, imaging and genetic findings in comparison with females. 12390976 2002
dbSNP: rs104894780
rs104894780
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT Subcortical band heterotopia (SBH) in males: clinical, imaging and genetic findings in comparison with females. 12390976 2002
dbSNP: rs104894781
rs104894781
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT Subcortical band heterotopia (SBH) in males: clinical, imaging and genetic findings in comparison with females. 12390976 2002
dbSNP: rs104894782
rs104894782
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT Subcortical band heterotopia (SBH) in males: clinical, imaging and genetic findings in comparison with females. 12390976 2002
dbSNP: rs104894783
rs104894783
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT Subcortical band heterotopia (SBH) in males: clinical, imaging and genetic findings in comparison with females. 12390976 2002
dbSNP: rs104894784
rs104894784
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT Subcortical band heterotopia (SBH) in males: clinical, imaging and genetic findings in comparison with females. 12390976 2002
dbSNP: rs104894785
rs104894785
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT Subcortical band heterotopia (SBH) in males: clinical, imaging and genetic findings in comparison with females. 12390976 2002
dbSNP: rs122457137
rs122457137
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT Subcortical band heterotopia (SBH) in males: clinical, imaging and genetic findings in comparison with females. 12390976 2002
dbSNP: rs104894779
rs104894779
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT Incomplete penetrance with normal MRI in a woman with germline mutation of the DCX gene. 11468322 2001