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 15 59295925 rs6494052 G A rs6494052 1.93E-04 Multiple complex diseases HPOID:0000118 NA G intron GWASdb_trait 15 59296076 rs10518995 C T rs10518995 1.64E-04 Type 2 diabetes HPOID:0005978 DOID:9352 C intron GWASdb_trait 15 59296491 rs1446240 G T rs1446240 1.90E-04 Asperger disorder HPOID:0000717 DOID:0050432 C intron GWASdb_trait 15 59353863 rs16940987 C A rs16940987 1.88E-11 Metabolite levels HPOID:0001939 DOID:655 C intron GWASdb_trait

Disease associated variation - OMIM Ensembl_gene_ID Approved Gene Symbol MIM Number ENSG00000157450.15 RNF111 605840