Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1554774575
rs1554774575
Entrez Id: 1759
Gene Symbol: DNM1
DNM1
CUI: C4225357
Disease:
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 31
A 0.700 CausalMutation CLINVAR