DCX, doublecortin, 1641

N. diseases: 175; N. variants: 107
Disease: Abnormal cortical gyration ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs797045519
rs797045519
Entrez Id: 1641
Gene Symbol: DCX
DCX
CUI: C1856019
Disease:
Abnormal cortical gyration 		GGGCTA 0.700 CausalMutation CLINVAR