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: rs797044556
rs797044556
Entrez Id: 1630;101928167
Gene Symbol: DCC;LINC01917
DCC;LINC01917
CUI: C0454455
Disease:
Mirror movements disorder 		A 0.700 CausalMutation CLINVAR A novel DCC mutation and genetic heterogeneity in congenital mirror movements. 21242494 2011