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 2 136506927 rs6430585 A C rs6430585 7.99E-04 Multiple complex diseases HPOID:0000118 NA C intron GWASdb_trait 2 136506927 rs6430585 A C rs6430585 1.78E-06 Paget's disease HPOID:0000924 DOID:5408 C intron GWASdb_trait 2 136506927 rs6430585 A C rs6430585 1.00E-06 Corneal structure HPOID:0000481 DOID:10124 C intron GWASdb_trait 2 136509460 rs16831992 G C rs16831992 1.90E-06 Phospholipid levels (plasma) HPOID:0003119 DOID:9352|DOID:3393 G intron GWASdb_trait 2 136522710 rs9287442 A G rs9287442 2.25E-06 Paget's disease HPOID:0000924 DOID:5408 A intron GWASdb_trait 2 136536113 rs10496736 C G rs10496736 1.60E-12 Health and aging, CVD and cancer age of onset HPOID:0002664|HPOID:0001626 DOID:1287|DOID:162 C intron GWASdb_trait 2 136536113 rs10496736 C G rs10496736 3.60E-14 Health and aging, CVD and cancer age of onset HPOID:0002664|HPOID:0001626 DOID:1287|DOID:162 C intron GWASdb_trait 2 136536113 rs10496736 C G rs10496736 4.80E-11 Health and aging, CVD and cancer age of onset HPOID:0002664|HPOID:0001626 DOID:1287|DOID:162 C intron GWASdb_trait 2 136542560 rs1469996 A G rs1469996 3.75E-06 Paget's disease HPOID:0000924 DOID:5408 A UTR-3 GWASdb_trait

Disease associated variation - OMIM Ensembl_gene_ID Approved Gene Symbol MIM Number ENSG00000144224.16 UBXN4 611216