PHRF1
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
11589564rs4963128TCrs49631283.00E-10Systemic lupus erythematosusHPOID:0002725DOID:9074AintronGWASdb_trait
11589564rs4963128TCrs49631284.00E-06Systemic lupus erythematosusHPOID:0002725DOID:9074AintronGWASdb_trait
11589564rs4963128TCrs49631284.90E-09Multiple sclerosisHPOID:0000096|HPOID:0001967|HPOID:0009741|HPOID:0008664|HPOID:0001150|HPOID:0005450|HPOID:0005652|HPOID:0005686|HPOID:0005789|HPOID:0100923|HPOID:0100925|HPOID:0006623|HPOID:0100861|HPOID:0002694|HPOID:0004979|HPOID:0003881|HPOID:0003991|HPOID:0003854|HPOID:0003933|HPOID:0004030|HPOID:0100899|HPOID:0002634DOID:2377AintronGWASdb_trait
11589564rs4963128TCrs49631282.50E-05Systemic lupus erythematosusHPOID:0002725DOID:9074AintronGWASdb_trait
11601785rs2396545TCrs23965458.00E-06Systemic lupus erythematosus and Systemic sclerosisHPOID:0002725DOID:9074|DOID:1578GintronGWASdb_trait
11606749rs936469GArs9364699.64E-07Systemic lupus erythematosus and Systemic sclerosisHPOID:0002725DOID:9074|DOID:1578CintronGWASdb_trait
11606749rs936469GArs9364699.33E-05Coronary heart diseaseHPOID:0001677DOID:3393CintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000070047.11 PHRF1 611780