KLHL21
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
16651728rs1556036CTrs15560361.06E-04Multiple complex diseasesHPOID:0000118NAGUTR-3GWASdb_trait
16651728rs1556036CTrs15560364.54E-05Heart RateHPOID:0005150|HPOID:0001645|HPOID:0001644|HPOID:0011704|HPOID:0005110DOID:10273GUTR-3GWASdb_trait
16657355rs4587589CTrs45875891.07E-04Multiple complex diseasesHPOID:0000118NACintronGWASdb_trait
Disease associated variation - GWAS Central
Study NameSource Marker AccessionChromosomeMarker StartMarker StopAllelesGene SectionP-value-log(p-value)
GWAS of prostate cancerrs201171166510936651093UTR30.4334510.363059990765404
GWAS of prostate cancerrs1556036166517286651728UTR30.2321550.634221958351348
GWAS of prostate cancerrs12028517166617326661732intronic0.1849210.7330137666869749
GWAS of prostate cancerrs6674407166629136662913UTR50.1729450.762091989323507
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000162413.16 KLHL21 616262