Disease: Absence Epilepsy ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4906902
rs4906902
Entrez Id: 2562
Gene Symbol: GABRB3
GABRB3
CUI: C0014553
Disease:
Absence Epilepsy 		0.020 GeneticVariation BEFREE However, allele frequencies of rs20317 and rs4906902 were not significantly associated with 48 rCAE patients in comparison to >500 controls matched for ethnicity and ancestral origin. 22765836 2012
dbSNP: rs4906902
rs4906902
Entrez Id: 2562
Gene Symbol: GABRB3
GABRB3
CUI: C0014553
Disease:
Absence Epilepsy 		0.020 GeneticVariation BEFREE Our study failed to replicate an association of the common GABRB3 exon 1a promoter SNP rs4906902 with CAE. 17215107 2007