RNF152
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
1859493334rs4319862GTrs43198623.83E-05Calcium intake levels and metabolic syndromeHPOID:0004363|HPOID:0002621|HPOID:0011915DOID:3146|DOID:4194|DOID:10763|DOID:14221|DOID:10575|DOID:1936GintronGWASdb_trait
1859494069rs8091174CTrs80911741.00E-04Osteoarthritis (knee and hip)HPOID:0002758DOID:8398CintronGWASdb_trait
1859494069rs8091174CTrs80911742.04E-05Osteoarthritis (knee and hip)HPOID:0002758DOID:8398CintronGWASdb_trait
1859494069rs8091174CTrs80911749.69E-05Osteoarthritis (knee and hip)HPOID:0002758DOID:8398CintronGWASdb_trait
1859504161rs9944883CArs99448833.19E-04Multiple complex diseasesHPOID:0000118NAAintronGWASdb_trait
1859505348rs4131216AGrs41312167.29E-04Multiple complex diseasesHPOID:0000118NATintronGWASdb_trait
1859550066rs9958268TArs99582684.66E-04Body mass indexHPOID:0001507DOID:9970AintronGWASdb_trait
1859550066rs9958268TArs99582681.71E-04Suicide attempts in bipolar disorderHPOID:0007302DOID:3312AintronGWASdb_trait
1859555405rs7505697GArs75056971.19E-04Body mass indexHPOID:0001507DOID:9970AintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000176641.10 RNF152 616512