Disease: Movement Disorders ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs752283089
rs752283089
Entrez Id: 23503
Gene Symbol: ZFYVE26
ZFYVE26
CUI: C0026650
Disease:
Movement Disorders 		T 0.700 GeneticVariation CLINVAR Exome sequencing in undiagnosed inherited and sporadic ataxias. 25497598 2015
dbSNP: rs752283089
rs752283089
Entrez Id: 23503
Gene Symbol: ZFYVE26
ZFYVE26
CUI: C0026650
Disease:
Movement Disorders 		T 0.700 GeneticVariation CLINVAR Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism. 24267886 2013