USP46
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
453457420rs2270827TCrs22708277.93E-04Acute lung injuryHPOID:0002088DOID:850AUTR-3GWASdb_trait
453459620rs3733506GArs37335067.93E-04Acute lung injuryHPOID:0002088DOID:850CUTR-3GWASdb_trait
453459731rs10034164AGrs100341647.33E-04Acute lung injuryHPOID:0002088DOID:850GUTR-3GWASdb_trait
453461980rs1053437ATrs10534371.33E-04Multiple complex diseasesHPOID:0000118NAAUTR-3GWASdb_trait
453463164rs7675404GCrs76754047.33E-04Acute lung injuryHPOID:0002088DOID:850CUTR-3GWASdb_trait
453463566rs17051586CTrs170515867.33E-04Acute lung injuryHPOID:0002088DOID:850TUTR-3GWASdb_trait
453465280rs6832794TCrs68327946.11E-04Acute lung injuryHPOID:0002088DOID:850T,CintronGWASdb_trait
453469343rs7687075CTrs76870756.11E-04Acute lung injuryHPOID:0002088DOID:850TintronGWASdb_trait
453471153rs7693087GArs76930876.52E-04Acute lung injuryHPOID:0002088DOID:850AintronGWASdb_trait
453472171rs7680727AGrs76807275.55E-04Acute lung injuryHPOID:0002088DOID:850AintronGWASdb_trait
453479414rs7671541CGrs76715419.43E-04Acute lung injuryHPOID:0002088DOID:850GintronGWASdb_trait
453483243rs7662693CGrs76626936.52E-04Acute lung injuryHPOID:0002088DOID:850CintronGWASdb_trait
453487541rs6554557TGrs65545576.52E-04Acute lung injuryHPOID:0002088DOID:850GintronGWASdb_trait
453498669rs10517263GCrs105172635.60E-04Acute lung injuryHPOID:0002088DOID:850GintronGWASdb_trait
453501531rs17051640ATrs170516406.67E-04Acute lung injuryHPOID:0002088DOID:850AintronGWASdb_trait
453506457rs10034052CTrs100340526.71E-04Acute lung injuryHPOID:0002088DOID:850TintronGWASdb_trait
453508927rs4865395GTrs48653956.71E-04Acute lung injuryHPOID:0002088DOID:850TintronGWASdb_trait
453513769rs7691678GArs76916785.77E-04Acute lung injuryHPOID:0002088DOID:850GintronGWASdb_trait
453523725rs10014556AGrs100145566.69E-04Acute lung injuryHPOID:0002088DOID:850GintronGWASdb_trait
453523832rs11939490AGrs119394905.40E-04Acute lung injuryHPOID:0002088DOID:850AintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000109189.12 USP46 612849