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

Disease associated variation - OMIM Ensembl_gene_ID Approved Gene Symbol MIM Number ENSG00000101557.14 USP14 607274