FBXW11
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
5171335293rs10475992CTrs104759923.00E-09HeightHPOID:0000002NACintronGWASdb_trait
5171350313rs839273AGrs8392732.30E-04Statin-induced myopathyHPOID:0001637DOID:0080000TintronGWASdb_trait
5171362662rs10040841CTrs100408417.17E-04Response to taxane treatment (placlitaxel)HPOID:0100526DOID:1324CintronGWASdb_trait
5171373215rs10475994CTrs104759947.17E-04Response to taxane treatment (placlitaxel)HPOID:0100526DOID:1324CintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000072803.17 FBXW11 605651