RNF10
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
12120974510rs614226CTrs6142262.00E-06Type 1 diabetes nephropathyHPOID:0100651DOID:9744|DOID:2370CintronGWASdb_trait
12120981471rs1167715TCrs11677156.03E-04Lymphocyte countsHPOID:0004332|HPOID:0002665DOID:2841|DOID:1240|DOID:0060058|DOID:614|DOID:1287AintronGWASdb_trait
12120992401rs3213565CTrs32135651.92E-04CholesterolHPOID:0003107DOID:2349|DOID:3393|DOID:3146GintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000022840.15 RNF10 615998