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 11 46422686 rs12574668 C A rs12574668 1.02E-08 Schizophrenia HPOID:0100753 DOID:5419 A intron GWASdb_trait 11 46442526 rs12283172 C T rs12283172 1.75E-04 Arthritis (juvenile idiopathic) HPOID:0005681 DOID:676 C intron GWASdb_trait 11 46484685 rs1472001 G A rs1472001 5.99E-04 Parkinson's disease HPOID:0001300 DOID:14330 G intron GWASdb_trait 11 46499874 rs7130141 C T rs7130141 6.96E-09 Schizophrenia HPOID:0100753 DOID:5419 T intron GWASdb_trait 11 46513249 rs7112229 C T rs7112229 7.38E-09 Schizophrenia HPOID:0100753 DOID:5419 C intron GWASdb_trait 11 46515004 rs12578042 C G rs12578042 7.83E-04 Multiple complex diseases HPOID:0000118 NA G intron GWASdb_trait 11 46560680 rs11819869 C T rs11819869 3.89E-09 Schizophrenia HPOID:0100753 DOID:5419 T intron GWASdb_trait 11 46561301 rs11038914 C T rs11038914 4.71E-04 Multiple complex diseases HPOID:0000118 NA T intron GWASdb_trait 11 46569272 rs7946801 G A rs7946801 1.26E-04 Multiple complex diseases HPOID:0000118 NA G intron GWASdb_trait

Disease associated variation - OMIM Ensembl_gene_ID Approved Gene Symbol MIM Number ENSG00000110497.14 AMBRA1 611359