DCC, DCC netrin 1 receptor, 1630

N. diseases: 279; N. variants: 101
Disease: Mirror movements disorder ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs797044552
rs797044552
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C0454455
Disease:
Mirror movements disorder 		TG 0.700 CausalMutation CLINVAR Mutations in DCC cause congenital mirror movements. 20431009 2010