Disease: Movement Disorders ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs875989786
rs875989786
Entrez Id: 10472
Gene Symbol: ZBTB18
ZBTB18
CUI: C0026650
Disease:
Movement Disorders 		T 0.700 GeneticVariation CLINVAR Delineation of a deletion region critical for corpus callosal abnormalities in chromosome 1q43-q44. 21934713 2012