Disease associated variation - GWASdb | Chr | Pos | SNP ID(dbSNP 142) | Ref | Alt | Ori SNP ID | P-value | Drug Name | Drug Anno | GWAS Trait | HPO ID | DO ID | AA | Type | Trait or Drug | 1 | 33421461 | rs194655 | T | C | rs194655 | 4.17E-04 | | | Multiple complex diseases | HPOID:0000118 | NA | A | intron | GWASdb_trait | |
Disease associated variation - GWAS Central | Study Name | Source Marker Accession | Chromosome | Marker Start | Marker Stop | Alleles | Gene Section | P-value | -log(p-value) | GWAS of prostate cancer | rs1149128 | 1 | 33408138 | 33408138 | | intronic | 0.352307 | 0.45307872772091 | GWAS of prostate cancer | rs194652 | 1 | 33419206 | 33419206 | | intronic | 0.24111 | 0.617784776952466 | GWAS of prostate cancer | rs194637 | 1 | 33401773 | 33401773 | | downstream | 0.196838 | 0.7058910563252989 | |
Disease associated variation - OMIM | Ensembl_gene_ID | Approved Gene Symbol | MIM Number | ENSG00000116514.16 | RNF19B | 610872 | |