DCX, doublecortin, 1641

N. diseases: 175; N. variants: 107
Disease: Lissencephaly, X-Linked, 1 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1556401951
rs1556401951
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C4551968
Disease:
Lissencephaly, X-Linked, 1 		A 0.700 CausalMutation CLINVAR