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: rs104894781
rs104894781
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT Genetic alteration of the DCX gene in Japanese patients with subcortical laminar heterotopia or isolated lissencephaly sequence. 10807542 2000
dbSNP: rs104894782
rs104894782
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT Genetic alteration of the DCX gene in Japanese patients with subcortical laminar heterotopia or isolated lissencephaly sequence. 10807542 2000
dbSNP: rs104894783
rs104894783
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT Genetic alteration of the DCX gene in Japanese patients with subcortical laminar heterotopia or isolated lissencephaly sequence. 10807542 2000
dbSNP: rs104894784
rs104894784
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT Genetic alteration of the DCX gene in Japanese patients with subcortical laminar heterotopia or isolated lissencephaly sequence. 10807542 2000
dbSNP: rs104894785
rs104894785
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT Genetic alteration of the DCX gene in Japanese patients with subcortical laminar heterotopia or isolated lissencephaly sequence. 10807542 2000
dbSNP: rs122457137
rs122457137
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT Genetic alteration of the DCX gene in Japanese patients with subcortical laminar heterotopia or isolated lissencephaly sequence. 10807542 2000
dbSNP: rs104894779
rs104894779
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT Characterization of mutations in the gene doublecortin in patients with double cortex syndrome. 9989615 1999
dbSNP: rs104894779
rs104894779
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT A novel mutation of the doublecortin gene in Japanese patients with X-linked lissencephaly and subcortical band heterotopia. 10369164 1999
dbSNP: rs104894779
rs104894779
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT Subcortical band heterotopia in rare affected males can be caused by missense mutations in DCX (XLIS) or LIS1. 10441340 1999
dbSNP: rs104894780
rs104894780
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT A novel mutation of the doublecortin gene in Japanese patients with X-linked lissencephaly and subcortical band heterotopia. 10369164 1999
dbSNP: rs104894780
rs104894780
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT Characterization of mutations in the gene doublecortin in patients with double cortex syndrome. 9989615 1999
dbSNP: rs104894780
rs104894780
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT Subcortical band heterotopia in rare affected males can be caused by missense mutations in DCX (XLIS) or LIS1. 10441340 1999
dbSNP: rs104894781
rs104894781
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT Characterization of mutations in the gene doublecortin in patients with double cortex syndrome. 9989615 1999
dbSNP: rs104894781
rs104894781
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT Subcortical band heterotopia in rare affected males can be caused by missense mutations in DCX (XLIS) or LIS1. 10441340 1999
dbSNP: rs104894781
rs104894781
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT A novel mutation of the doublecortin gene in Japanese patients with X-linked lissencephaly and subcortical band heterotopia. 10369164 1999
dbSNP: rs104894782
rs104894782
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT Subcortical band heterotopia in rare affected males can be caused by missense mutations in DCX (XLIS) or LIS1. 10441340 1999
dbSNP: rs104894782
rs104894782
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT A novel mutation of the doublecortin gene in Japanese patients with X-linked lissencephaly and subcortical band heterotopia. 10369164 1999
dbSNP: rs104894782
rs104894782
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT Characterization of mutations in the gene doublecortin in patients with double cortex syndrome. 9989615 1999
dbSNP: rs104894783
rs104894783
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT Subcortical band heterotopia in rare affected males can be caused by missense mutations in DCX (XLIS) or LIS1. 10441340 1999
dbSNP: rs104894783
rs104894783
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT Characterization of mutations in the gene doublecortin in patients with double cortex syndrome. 9989615 1999
dbSNP: rs104894783
rs104894783
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT A novel mutation of the doublecortin gene in Japanese patients with X-linked lissencephaly and subcortical band heterotopia. 10369164 1999
dbSNP: rs104894784
rs104894784
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT A novel mutation of the doublecortin gene in Japanese patients with X-linked lissencephaly and subcortical band heterotopia. 10369164 1999
dbSNP: rs104894784
rs104894784
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT Characterization of mutations in the gene doublecortin in patients with double cortex syndrome. 9989615 1999
dbSNP: rs104894784
rs104894784
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT Subcortical band heterotopia in rare affected males can be caused by missense mutations in DCX (XLIS) or LIS1. 10441340 1999
dbSNP: rs104894785
rs104894785
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		0.800 GeneticVariation UNIPROT Characterization of mutations in the gene doublecortin in patients with double cortex syndrome. 9989615 1999