Disease associated variation - GWASdb | Chr | Pos | SNP ID(dbSNP 142) | Ref | Alt | Ori SNP ID | P-value | Drug Name | Drug Anno | GWAS Trait | HPO ID | DO ID | AA | Type | Trait or Drug | 18 | 196829 | rs655781 | G | A | rs655781 | 1.56E-04 | | | Epilepsy | HPOID:0001250 | DOID:1826 | A | intron | GWASdb_trait | 18 | 204232 | rs585578 | G | A | rs585578 | 1.40E-04 | | | Epilepsy | HPOID:0001250 | DOID:1826 | T | intron | GWASdb_trait | |