UBE2R2
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
933820938rs10971712CTrs109717121.21E-04Alzheimer's disease (late onset)HPOID:0002511DOID:10652TintronGWASdb_trait
933841798rs10971733GArs109717331.89E-04Type 2 diabetesHPOID:0005978DOID:9352GintronGWASdb_trait
933853118rs13295276GArs132952762.07E-06IgE levelsHPOID:0010701DOID:6024GintronGWASdb_trait
933869781rs10971750TCrs109717501.21E-04Alzheimer's disease (late onset)HPOID:0002511DOID:10652TintronGWASdb_trait
933870940rs7856487GArs78564871.21E-04Alzheimer's disease (late onset)HPOID:0002511DOID:10652AintronGWASdb_trait
933873557rs6476426CGrs64764264.89E-04Type 2 diabetesHPOID:0005978DOID:9352CintronGWASdb_trait
933888000rs13302810CArs133028107.98E-06IgE levelsHPOID:0010701DOID:6024CintronGWASdb_trait
933898779rs10971773GArs109717731.21E-04Alzheimer's disease (late onset)HPOID:0002511DOID:10652AintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000107341.4 UBE2R2 612506