KLHL8
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
488126218rs17012552CTrs170125521.21E-04Coronary heart diseaseHPOID:0001677DOID:3393CintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000145332.13 KLHL8 611967