Disease: Amish Infantile Epilepsy Syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs778265926
rs778265926
Entrez Id: 8869
Gene Symbol: ST3GAL5
ST3GAL5
CUI: C1836824
Disease:
Amish Infantile Epilepsy Syndrome 		T 0.700 CausalMutation CLINVAR