RNF19B
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
133421461rs194655TCrs1946554.17E-04Multiple complex diseasesHPOID:0000118NAAintronGWASdb_trait
Disease associated variation - GWAS Central
Study NameSource Marker AccessionChromosomeMarker StartMarker StopAllelesGene SectionP-value-log(p-value)
GWAS of prostate cancerrs114912813340813833408138intronic0.3523070.45307872772091
GWAS of prostate cancerrs19465213341920633419206intronic0.241110.617784776952466
GWAS of prostate cancerrs19463713340177333401773downstream0.1968380.7058910563252989
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000116514.16 RNF19B 610872