ARX, aristaless related homeobox, 170302

N. diseases: 249; N. variants: 44
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 1 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587783191
rs587783191
Entrez Id: 170302
Gene Symbol: ARX
ARX
CUI: C3463992
Disease:
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 1 		G 0.700 CausalMutation CLINVAR