Source: UNIPROT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121909673
rs121909673
GABRG2
CUI: C1843244
Disease: EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2
EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2 		0.800 GeneticVariation UNIPROT Mutant GABA(A) receptor gamma2-subunit in childhood absence epilepsy and febrile seizures. 11326275

2001