Disease: Epilepsy, Partial, with Variable Foci ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587777458
rs587777458
Entrez Id: 9681
Gene Symbol: DEPDC5
DEPDC5
CUI: C1858477
Disease:
Epilepsy, Partial, with Variable Foci 		T 0.700 CausalMutation CLINVAR DEPDC5 mutations in families presenting as autosomal dominant nocturnal frontal lobe epilepsy. 24814846 2014