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: rs797044554
rs797044554
Entrez Id: 1630
Gene Symbol: DCC
DCC
CUI: C0454455
Disease:
Mirror movements disorder 		TCCAG 0.700 CausalMutation CLINVAR Congenital mirror movements: mutational analysis of RAD51 and DCC in 26 cases. 24808016 2014