FBXO22
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
1576196674rs2455895TCrs24558951.09E-04Multiple complex diseasesHPOID:0000118NAGintronGWASdb_trait
1576217098rs1695372TCrs16953725.28E-05Multiple complex diseasesHPOID:0000118NAGintronGWASdb_trait
1576218414rs2648436TGrs26484361.11E-04Multiple complex diseasesHPOID:0000118NACintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000167196.13 FBXO22 609096