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 10 99271281 rs10786352 C T rs10786352 2.47E-04 Hemoglobin concentration HPOID:0011902 DOID:2860 C intron GWASdb_trait 10 99278820 rs7908417 T C rs7908417 2.39E-04 Amyotrophic lateral sclerosis (sporadic) HPOID:0007354 DOID:332 C intron GWASdb_trait 10 99281872 rs4917774 A G rs4917774 6.15E-05 Serum metabolites HPOID:0011111 NA G intron GWASdb_trait 10 99283062 rs11592144 T G rs11592144 4.98E-04 Hemoglobin concentration HPOID:0011902 DOID:2860 T intron GWASdb_trait 10 99294797 rs12767760 G A rs12767760 7.00E-06 Obesity-related traits HPOID:0001513 DOID:9970 G intron GWASdb_trait 10 99317388 rs2185512 A G rs2185512 3.42E-04 Insulin resistance HPOID:0000855 DOID:9352 G intron GWASdb_trait

Disease associated variation - OMIM Ensembl_gene_ID Approved Gene Symbol MIM Number ENSG00000165886.4 UBTD1 616388