PRKAA1
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
540767397rs1002424AGrs10024245.21E-10SchizophreniaHPOID:0100753DOID:5419TintronGWASdb_trait
540775297rs3792822CTrs37928229.80E-04Major depressive disorderHPOID:0000716DOID:1470GintronGWASdb_trait
540790551rs10074991GArs100749912.54E-04Multiple complex diseasesHPOID:0000118NAAintronGWASdb_trait
540790551rs10074991GArs100749917.10E-04Major depressive disorderHPOID:0000716DOID:1470AintronGWASdb_trait
540790551rs10074991GArs100749911.94E-04Autism spectrum disorders (language delay)HPOID:0000729DOID:0060041AintronGWASdb_trait
540790551rs10074991GArs100749915.11E-05Parkinson's diseaseHPOID:0001300DOID:14330AintronGWASdb_trait
540790551rs10074991GArs100749914.21E-10SchizophreniaHPOID:0100753DOID:5419AintronGWASdb_trait
540791884rs13361707CTrs133617072.25E-04Multiple complex diseasesHPOID:0000118NACintronGWASdb_trait
540791884rs13361707CTrs133617076.80E-04Major depressive disorderHPOID:0000716DOID:1470CintronGWASdb_trait
540791884rs13361707CTrs133617072.30E-05Urinary metabolitesHPOID:0000079DOID:557CintronGWASdb_trait
540791884rs13361707CTrs133617078.00E-29Gastric cancerHPOID:0012126DOID:3717CintronGWASdb_trait
540791884rs13361707CTrs133617077.77E-08SchizophreniaHPOID:0100753DOID:5419CintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000132356.11 PRKAA1 602739