DNM1, dynamin 1, 1759

N. diseases: 114; N. variants: 19
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 31 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1554772959
rs1554772959
Entrez Id: 1759
Gene Symbol: DNM1
DNM1
CUI: C4225357
Disease:
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 31 		G 0.700 GeneticVariation CLINVAR [Dynamin-1-related infantile spasms: a case report and review of literature]. 27806796 2016