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: rs104894782
rs104894782
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C1848070
Disease:
Lissencephaly and agenesis of corpus callosum 		C 0.700 CausalMutation CLINVAR