FBXL20
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
1737409865rs755500GArs7555001.70E-05Urinary metabolitesHPOID:0000079DOID:557AUTR-3GWASdb_trait
1737409865rs755500GArs7555009.18E-07Red blood cell traitsHPOID:0001877DOID:74AUTR-3GWASdb_trait
1737419317rs2338755TCrs23387551.50E-05Urinary metabolitesHPOID:0000079DOID:557AintronGWASdb_trait
1737419317rs2338755TCrs23387558.35E-07Red blood cell traitsHPOID:0001877DOID:74AintronGWASdb_trait
1737424149rs8073907CTrs80739073.50E-07Primary biliary cirrhosisHPOID:0002613DOID:12236TintronGWASdb_trait
1737424149rs8073907CTrs80739072.40E-07Red blood cell traitsHPOID:0001877DOID:74TintronGWASdb_trait
1737436966rs634365CTrs6343651.40E-05Urinary metabolitesHPOID:0000079DOID:557GintronGWASdb_trait
1737439496rs602688TCrs6026881.20E-05Urinary metabolitesHPOID:0000079DOID:557GintronGWASdb_trait
1737439496rs602688TCrs6026889.89E-07Red blood cell traitsHPOID:0001877DOID:74GintronGWASdb_trait
1737441109rs801426GArs8014261.50E-05Urinary metabolitesHPOID:0000079DOID:557TintronGWASdb_trait
1737441109rs801426GArs8014268.93E-07Red blood cell traitsHPOID:0001877DOID:74TintronGWASdb_trait
1737444036rs585961GArs5859613.56E-04Alcohol dependenceHPOID:0000707DOID:0050741TintronGWASdb_trait
1737446571rs590051TCrs5900513.50E-07Primary biliary cirrhosisHPOID:0002613DOID:12236AintronGWASdb_trait
1737453294rs632202CArs6322023.13E-07Red blood cell traitsHPOID:0001877DOID:74TintronGWASdb_trait
1737457342rs2302073AGrs23020732.40E-07Primary biliary cirrhosisHPOID:0002613DOID:12236TintronGWASdb_trait
1737477218rs8066704CTrs80667049.94E-07Red blood cell traitsHPOID:0001877DOID:74TintronGWASdb_trait
1737478062rs8070695GArs80706951.50E-05Urinary metabolitesHPOID:0000079DOID:557AintronGWASdb_trait
1737478062rs8070695GArs80706955.79E-07Red blood cell traitsHPOID:0001877DOID:74AintronGWASdb_trait
1737483599rs9944411TCrs99444118.37E-07Chronic kidney diseaseHPOID:0000077DOID:784TintronGWASdb_trait
1737483599rs9944411TCrs99444118.00E-07Red blood cell traitsHPOID:0001877DOID:74TintronGWASdb_trait
1737487168rs7220650TCrs72206505.72E-04Alcohol dependenceHPOID:0000707DOID:0050741CintronGWASdb_trait
1737487168rs7220650TCrs72206501.40E-05Urinary metabolitesHPOID:0000079DOID:557CintronGWASdb_trait
1737487168rs7220650TCrs72206503.20E-07Red blood cell traitsHPOID:0001877DOID:74CintronGWASdb_trait
1737498149rs2338800GCrs23388003.45E-04Multiple complex diseasesHPOID:0000118NAGintronGWASdb_trait
1737498149rs2338800GCrs23388001.90E-05Urinary metabolitesHPOID:0000079DOID:557GintronGWASdb_trait
1737498149rs2338800GCrs23388003.66E-07Red blood cell traitsHPOID:0001877DOID:74GintronGWASdb_trait
1737499949rs9916302TCrs99163025.42E-07Red blood cell traitsHPOID:0001877DOID:74TintronGWASdb_trait
1737504933rs8069451TCrs80694518.20E-04Alcohol dependenceHPOID:0000707DOID:0050741CintronGWASdb_trait
1737504933rs8069451TCrs80694511.60E-05Urinary metabolitesHPOID:0000079DOID:557CintronGWASdb_trait
1737504933rs8069451TCrs80694512.70E-07Red blood cell traitsHPOID:0001877DOID:74CintronGWASdb_trait
1737516722rs8076494TCrs80764941.60E-05Urinary metabolitesHPOID:0000079DOID:557TintronGWASdb_trait
1737516722rs8076494TCrs80764946.97E-07Red blood cell traitsHPOID:0001877DOID:74TintronGWASdb_trait
1737520449rs9908131TCrs99081312.40E-07Primary biliary cirrhosisHPOID:0002613DOID:12236TintronGWASdb_trait
1737532916rs4511574CTrs45115744.64E-04Alcohol dependenceHPOID:0000707DOID:0050741TintronGWASdb_trait
1737543328rs7221875GArs72218759.32E-07Red blood cell traitsHPOID:0001877DOID:74AintronGWASdb_trait
1737543449rs7208487TGrs72084878.00E-07Primary biliary cirrhosisHPOID:0002613DOID:12236TintronGWASdb_trait
1737543449rs7208487TGrs72084875.60E-09Glomerular filtration rateHPOID:0012212DOID:557TintronGWASdb_trait
1737547631rs9906612ACrs99066122.40E-07Primary biliary cirrhosisHPOID:0002613DOID:12236AintronGWASdb_trait
1737555403rs8076546GArs80765462.63E-07Red blood cell traitsHPOID:0001877DOID:74AintronGWASdb_trait
1737556431rs9904919GCrs99049192.57E-07Red blood cell traitsHPOID:0001877DOID:74CintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000108306.11 FBXL20 609086