RNF24
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
203934766rs6084530CArs60845307.75E-04Smoking cessationHPOID:0000707DOID:0050742AintronGWASdb_trait
203939140rs2253977TCrs22539775.27E-05Blood PressureHPOID:0011025DOID:10763AintronGWASdb_trait
203946057rs2300216AGrs23002168.12E-04Depression (quantitative trait)HPOID:0000716DOID:1596TintronGWASdb_trait
203965054rs998132GArs9981323.96E-06Blood PressureHPOID:0011025DOID:10763CintronGWASdb_trait
203972793rs6052222GArs60522225.59E-04Acute lung injuryHPOID:0002088DOID:850AintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000101236.16 RNF24 612489