DMXL1
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
5118435127rs116348108AGrs1163481089.00E-07Alzheimer's disease (cognitive decline)HPOID:0002511DOID:10652AintronGWASdb_trait
5118474109rs4895185AGrs48951851.69E-04Anorexia nervosaHPOID:0002039DOID:8689AintronGWASdb_trait
5118474205rs4895361AGrs48953612.26E-05Brain structureHPOID:0007319DOID:10652GintronGWASdb_trait
5118481205rs7717384GArs77173845.68E-04Alcohol consumption (maxi-drinks)HPOID:0000707DOID:1574|DOID:0050741GintronGWASdb_trait
5118516878rs3923326GArs39233261.70E-05Urinary metabolitesHPOID:0000079DOID:557CintronGWASdb_trait
5118530872rs3992620AGrs39926206.10E-04Type 2 diabetesHPOID:0005978DOID:9352AintronGWASdb_trait
5118530872rs3992620AGrs39926207.79E-04Multiple complex diseasesHPOID:0000118NAAintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000172869.14 DMXL1 605671