DCX, doublecortin, 1641

N. diseases: 175; N. variants: 107
Disease: Malformations of Cortical Development, Group II ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587783530
rs587783530
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C1837249
Disease:
Malformations of Cortical Development, Group II 		C 0.700 GeneticVariation CLINVAR