CCNB1IP1
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
1420781361rs2297732AGrs22977321.96E-05SchizophreniaHPOID:0100753DOID:5419GintronGWASdb_trait
1420782165rs10131909TCrs101319098.16E-05SchizophreniaHPOID:0100753DOID:5419TintronGWASdb_trait
1420796878rs8022565TCrs80225659.24E-05Multiple complex diseasesHPOID:0000118NATintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000100814.17 CCNB1IP1 608249