KLHL14
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
1830301116rs9954988CArs99549881.09E-04Multiple complex diseasesHPOID:0000118NACintronGWASdb_trait
1830340360rs12606529TCrs126065294.91E-04Iron levelsHPOID:0011031DOID:2351TintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000197705.9 KLHL14 613772