DENND3
Disease associated variation - ClinVar
Allele IDTypeNameRS#dbSNPPhenotype IDsChromosomeStartStopReferenceAlternate
362049deletionNM_014957.2(DENND3):c.1920delG (p.Lys640Asnfs)-1MedGen:C2931876,OMIM:1426238142178509142178509G-
362049deletionNM_014957.2(DENND3):c.1920delG (p.Lys640Asnfs)-1MedGen:C2931876,OMIM:1426238141168410141168410G-
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
8142138860rs3739232CGrs37392324.12E-06Intracerebral hemorrhageHPOID:0001342DOID:6713CUTR-5GWASdb_trait
8142139187rs3739231CTrs37392314.56E-06Intracerebral hemorrhageHPOID:0001342DOID:6713AintronGWASdb_trait
8142139251rs6578152TCrs65781526.33E-06Intracerebral hemorrhageHPOID:0001342DOID:6713CintronGWASdb_trait
8142151713rs307766CTrs3077666.60E-04Alcohol dependenceHPOID:0000707DOID:0050741AintronGWASdb_trait
8142161064rs3816063CG,Trs38160632.00E-06Obesity-related traitsHPOID:0001513DOID:9970GintronGWASdb_trait
8142198596rs7001673GTrs70016734.97E-09NarcolepsyHPOID:0100786DOID:8986TintronGWASdb_trait
8142198596rs7001673GTrs70016737.58E-04Body mass indexHPOID:0001507DOID:9970TintronGWASdb_trait
8142198682rs6988366TCrs69883661.50E-05Urinary metabolitesHPOID:0000079DOID:557TintronGWASdb_trait
8142198682rs6988366TCrs69883663.09E-04Body mass indexHPOID:0001507DOID:9970TintronGWASdb_trait
8142198682rs6988366TCrs69883663.71E-04Body mass indexHPOID:0001507DOID:9970TintronGWASdb_trait
8142201477rs13270024TCrs132700243.29E-04Attention deficit hyperactivity disorderHPOID:0007018DOID:1094TintronGWASdb_trait
8142205237rs9792AGrs97927.98E-04Body mass indexHPOID:0001507DOID:9970CUTR-3GWASdb_trait