Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1556607762
rs1556607762
Entrez Id: 9681
Gene Symbol: DEPDC5
DEPDC5
CUI: C1858477
Disease:
Epilepsy, Partial, with Variable Foci
T 0.700 GeneticVariation CLINVAR