Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1554781553
rs1554781553
Entrez Id: 1759
Gene Symbol: DNM1
DNM1
CUI: C4225357
Disease:
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 31
G 0.700 GeneticVariation CLINVAR