RNF123
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
349735746rs11130214CGrs111302146.74E-05Multiple complex diseasesHPOID:0000118NACintronGWASdb_trait
349735746rs11130214CGrs111302148.10E-04Bipolar disorder, schizoaffectiveHPOID:0007302|HPOID:0100753DOID:3312|DOID:5418CintronGWASdb_trait
349738945rs6804655CTrs68046553.80E-04Coronary heart diseaseHPOID:0001677DOID:3393Ccds-synonGWASdb_trait
349751585rs2291542CTrs22915425.32E-05Multiple complex diseasesHPOID:0000118NAGcds-synonGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000164068.15 RNF123 614472