FBXO8
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
4175162649rs7681841CTrs76818417.80E-06Urinary metabolitesHPOID:0000079DOID:557TintronGWASdb_trait
4175168083rs6824643GArs68246437.57E-05Amyotrophic Lateral SclerosisHPOID:0007354DOID:332GintronGWASdb_trait
4175168153rs6851312AGrs68513127.34E-05Amyotrophic Lateral SclerosisHPOID:0007354DOID:332AintronGWASdb_trait
4175168153rs6851312AGrs68513121.87E-04Lung function (forced expiratory volume in 1 second to forced vital capacity ratio)HPOID:0002088DOID:850AintronGWASdb_trait
4175183493rs10520276TCrs105202762.72E-04Amyotrophic Lateral SclerosisHPOID:0007354DOID:332TintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000164117.13 FBXO8 605649