FBXW8
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
12117424506rs11068277TArs110682773.07E-08Lymphocyte countsHPOID:0004332|HPOID:0002665DOID:2841|DOID:1240|DOID:0060058|DOID:614|DOID:1287TintronGWASdb_trait
12117436861rs4767492CTrs47674929.49E-04Brain structureHPOID:0007319DOID:10652TintronGWASdb_trait
12117436861rs4767492CTrs47674923.50E-07Hippocampal volumeHPOID:0002511DOID:10652TintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000174989.12 FBXW8 609073