RNF114
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
2048554977rs2235617CGrs22356178.80E-06Parkinson's diseaseHPOID:0001300DOID:14330GintronGWASdb_trait
2048554977rs2235617CGrs22356172.00E-06PsoriasisHPOID:0003765DOID:8893GintronGWASdb_trait
2048556229rs1056198CTrs10561982.16E-05Parkinson's diseaseHPOID:0001300DOID:14330CintronGWASdb_trait
2048556229rs1056198CTrs10561981.50E-14PsoriasisHPOID:0003765DOID:8893CintronGWASdb_trait
2048568929rs6125829GTrs61258291.40E-05Parkinson's diseaseHPOID:0001300DOID:14330GUTR-3GWASdb_trait
2048569127rs2235616GArs22356161.41E-05Parkinson's diseaseHPOID:0001300DOID:14330CUTR-3GWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000124226.10 RNF114 612451