Disease Term Disease ID Gene Symbol Classification References Source
Benign Rolandic Epilepsy C2363129 KCNQ2 Causal Pathogenic evidence from ClinVar 18625963, 18640800, 22884718 ClinVar
GABRG2 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 25726841 -
GRIN2A Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 23933819 -
SRPX2 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -