RNF139
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
8125488907rs4330675CTrs43306756.14E-04Alzheimer's diseaseHPOID:0002511DOID:10652CintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000170881.4 RNF139 603046