UHRF2
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
96447196rs560059GArs5600594.89E-07SERUM ALBUMINTNFRSF13B PROTEIN, HUMAN|IMMUNOGLOBULIN ISOTYPES|TRANSMEMBRANE ACTIVATOR AND CAML INTERACTOR PROTEIN|BLOOD PROTEINS|ANNEXIN A3|TNFSF13 PROTEIN, HUMAN|TUMOR NECROSIS FACTOR LIGAND SUPERFAMILY MEMBER 13Non-albumin protein levelsHPOID:0010876NAAintronGWASdb_drug
96414839rs10975580AGrs109755803.57E-06Rheumatoid arthritisHPOID:0001370DOID:7148AintronGWASdb_trait
96429259rs10975587GArs109755876.99E-05Cognitive test performanceHPOID:0100543DOID:1561GintronGWASdb_trait
96432156rs10739103CArs107391034.92E-04Multiple complex diseasesHPOID:0000118NAAintronGWASdb_trait
96447196rs560059GArs5600594.89E-07Non-albumin protein levelsHPOID:0010876NAAintronGWASdb_trait
96451088rs7027361GArs70273612.50E-05Parkinson's disease (age of onset)HPOID:0001300DOID:14330AintronGWASdb_trait
96469964rs7869419TGrs78694199.64E-04Multiple complex diseasesHPOID:0000118NATintronGWASdb_trait
96486308rs16924631GCrs169246313.00E-06Periodontal microbiotaHPOID:0000168DOID:824GintronGWASdb_trait
96492715rs13290126GArs132901262.62E-04Multiple complex diseasesHPOID:0000118NAAintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000147854.16 UHRF2 615211