Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 52 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894718
rs104894718
Entrez Id: 6324
Gene Symbol: SCN1B
SCN1B
CUI: C4479236
Disease:
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 52 		G 0.700 GeneticVariation CLINVAR