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 | 2 | 32713706 | rs2366894 | A | T | rs2366894 | 9.43E-04 | | | Parkinson's disease | HPOID:0001300 | DOID:14330 | T | missense | 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 | rs6543658 | 2 | 32718849 | 32718849 | | intronic | 0.819835 | 0.08627354493339859 | GWAS of prostate cancer | rs2754513 | 2 | 32782763 | 32782763 | | intronic | 0.714752 | 0.145844620737027 | GWAS of prostate cancer | rs12992095 | 2 | 32661543 | 32661543 | | intronic | 0.697242 | 0.156616460031847 | GWAS of prostate cancer | rs3769598 | 2 | 32679732 | 32679732 | | intronic | 0.660117 | 0.180379082714065 | |
Disease associated variation - OMIM | Ensembl_gene_ID | Approved Gene Symbol | MIM Number | ENSG00000115760.13 | BIRC6 | 605638 | |