rs1057519389, EBF3

N. diseases: 46
Disease: Dysarthria ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Dysarthria
CUI: C0013362
Disease: Dysarthria
0.700 CausalMutation CLINVAR A Syndromic Neurodevelopmental Disorder Caused by De Novo Variants in EBF3. 28017372 2017