MIDN
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
191250109rs3746106CArs37461068.90E-05Glucose levelsHPOID:0000819DOID:9352CUTR-5GWASdb_trait
191250109rs3746106CArs37461064.72E-05Glucose levelsHPOID:0000819DOID:9352CUTR-5GWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000167470.12 MIDN 606700