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 8 30601805 rs2278092 C T rs2278092 2.17E-04 Body mass index HPOID:0001507 DOID:9970 G intron GWASdb_trait 8 30601805 rs2278092 C T rs2278092 4.50E-04 Body mass index HPOID:0001507 DOID:9970 G intron GWASdb_trait 8 30607588 rs2911691 C G rs2911691 2.14E-04 Body mass index HPOID:0001507 DOID:9970 G intron GWASdb_trait 8 30607588 rs2911691 C G rs2911691 3.27E-04 Body mass index HPOID:0001507 DOID:9970 G intron GWASdb_trait 8 30607588 rs2911691 C G rs2911691 7.22E-04 Body mass index HPOID:0001507 DOID:9970 G intron GWASdb_trait 8 30607671 rs12156104 C T rs12156104 2.15E-04 Body mass index HPOID:0001507 DOID:9970 C intron GWASdb_trait 8 30607671 rs12156104 C T rs12156104 3.30E-04 Body mass index HPOID:0001507 DOID:9970 C intron GWASdb_trait 8 30607671 rs12156104 C T rs12156104 8.14E-04 Body mass index HPOID:0001507 DOID:9970 C intron GWASdb_trait

Disease associated variation - OMIM Ensembl_gene_ID Approved Gene Symbol MIM Number ENSG00000104691.14 UBXN8 602155