Disease: Epilepsy ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs16969925
rs16969925
Entrez Id: 6324
Gene Symbol: SCN1B
SCN1B
CUI: C0014544
Disease:
Epilepsy 		0.010 GeneticVariation BEFREE In contrast, two other SCN1B mutations associated with epilepsy, p.C121W and p.R85H, are expressed at the cell surface. 21994374 2011