FBXL2
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
333336370rs7628482CTrs76284820.0005823INFLIXIMAB|ADALIMUMAB|IMMUNOGLOBULIN GTUMOR NECROSIS FACTOR-ALPHA|ANTIRHEUMATIC AGENTS|ANTIBODIES, MONOCLONAL, HUMANIZED|TNFR-FC FUSION PROTEIN|ANTIBODIES, MONOCLONAL|RECEPTORS, TUMOR NECROSIS FACTORAnti-TNF treatment response in rheumatoid arthritis (by DAS-28 score change at 3 months)HPOID:0001370DOID:7148CintronGWASdb_drug
333336370rs7628482CTrs76284825.82E-04LEUCOVORIN|METHOTREXATESLCO1B1 PROTEIN, HUMAN|ORGANIC ANION TRANSPORTERSMethotrexate clearance (acute lymphoblastic leukemia)HPOID:0006721DOID:9952|DOID:12603CintronGWASdb_drug
333336370rs7628482CTrs76284820.0005823Anti-TNF treatment response in rheumatoid arthritis (by DAS-28 score change at 3 months)HPOID:0001370DOID:7148CintronGWASdb_trait
333336370rs7628482CTrs76284825.82E-04Methotrexate clearance (acute lymphoblastic leukemia)HPOID:0006721DOID:9952|DOID:12603CintronGWASdb_trait
333388184rs6769005TArs67690058.13E-04Multiple complex diseasesHPOID:0000118NAAintronGWASdb_trait
333413263rs4678929TGrs46789291.73E-05Behcet's diseaseHPOID:0011955DOID:13241TintronGWASdb_trait
333419422rs2291897CTrs22918971.47E-05Behcet's diseaseHPOID:0011955DOID:13241GintronGWASdb_trait
333419422rs2291897CTrs22918971.82E-05Behcet's diseaseHPOID:0011955DOID:13241GintronGWASdb_trait
333421178rs4045539ACrs40455391.56E-05Behcet's diseaseHPOID:0011955DOID:13241TintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000153558.13 FBXL2 605652