Disease: EPILEPSY, CHILDHOOD ABSENCE, 1 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1567106381
rs1567106381
Entrez Id: 2562
Gene Symbol: GABRB3
GABRB3
CUI: C1838604
Disease:
EPILEPSY, CHILDHOOD ABSENCE, 1 		G 0.700 GeneticVariation CLINVAR