UHRF1
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
194953351rs1982468TGrs19824681.62E-04TAMOXIFENANTINEOPLASTIC AGENTS, HORMONALResponse to tamoxifen in breast cancerHPOID:0003002DOID:0050671GintronGWASdb_drug
194915938rs2602707CTrs26027073.55E-04Multiple complex diseasesHPOID:0000118NAGintronGWASdb_trait
194929473rs2123731AGrs21237317.50E-17Progranulin levelsHPOID:0011018DOID:9255Gcds-synonGWASdb_trait
194929473rs2123731AGrs21237317.50E-17Myocardial infarctionHPOID:0001658DOID:5844Gcds-synonGWASdb_trait
194933777rs8107449GArs81074491.17E-04Iron levelsHPOID:0011031DOID:2351TintronGWASdb_trait
194953351rs1982468TGrs19824681.62E-04Response to tamoxifen in breast cancerHPOID:0003002DOID:0050671GintronGWASdb_trait
194958380rs881416CTrs8814163.46E-04Smoking initiationHPOID:0000707DOID:0050742TintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000276043.4 UHRF1 607990