RNF181
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
285824251rs6643TCrs66436.58E-04Glycosylated haemoglobin levelsHPOID:0011902|HPOID:0000077|HPOID:0001626|HPOID:0000819|HPOID:0000479DOID:1287|DOID:9351|DOID:557|DOID:5679CmissenseGWASdb_trait
285824468rs2232750CTrs22327507.06E-05Lymphocyte countsHPOID:0004332|HPOID:0002665DOID:2841|DOID:1240|DOID:0060058|DOID:614|DOID:1287CintronGWASdb_trait
Disease associated variation - GWAS Central
Study NameSource Marker AccessionChromosomeMarker StartMarker StopAllelesGene SectionP-value-log(p-value)
GWAS of prostate cancerrs664328582425185824251exonic0.8791240.0559498635864758
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000168894.9 RNF181 612490