HCK
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
2030673424rs242609CTrs2426097.27E-04Multiple complex diseasesHPOID:0000118NACintronGWASdb_trait
2030677208rs6089170CTrs60891706.79E-08Metabolite levelsHPOID:0001939DOID:655TintronGWASdb_trait
2030680338rs926688GTrs9266886.71E-08Metabolite levelsHPOID:0001939DOID:655TintronGWASdb_trait
2030681543rs980368AGrs9803686.71E-08Metabolite levelsHPOID:0001939DOID:655GintronGWASdb_trait
2030681999rs6121337TCrs61213376.71E-08Metabolite levelsHPOID:0001939DOID:655CintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000101336.12 HCK 142370