UBTD2
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
5171638165rs17701158TCrs177011581.75E-04CholesterolHPOID:0003107DOID:2349|DOID:3393|DOID:3146TUTR-3GWASdb_trait
5171649347rs17074475TArs170744757.63E-04Multiple complex diseasesHPOID:0000118NATintronGWASdb_trait
5171653121rs41495146TGrs414951466.37E-04Multiple complex diseasesHPOID:0000118NATintronGWASdb_trait
5171656546rs13165241TCrs131652418.91E-05CholesterolHPOID:0003107DOID:2349|DOID:3393|DOID:3146TintronGWASdb_trait
5171658346rs12659926AGrs126599269.22E-04Multiple complex diseasesHPOID:0000118NAAintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000168246.5 UBTD2 610174