rs398123812, CASD1;SGCE

N. diseases: 1
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Myoclonic dystonia
CUI: C1834570
Disease: Myoclonic dystonia
0.700 CausalMutation CLINVAR Myoclonus-dystonia: significance of large SGCE deletions. 18205193 2008