Disease associated variation - ClinVar Allele ID Type Name RS#dbSNP Phenotype IDs Chromosome Start Stop Reference Alternate 362049 deletion NM_014957.2(DENND3):c.1920delG (p.Lys640Asnfs) -1 MedGen:C2931876,OMIM:142623 8 142178509 142178509 G - 362049 deletion NM_014957.2(DENND3):c.1920delG (p.Lys640Asnfs) -1 MedGen:C2931876,OMIM:142623 8 141168410 141168410 G -

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 8 142138860 rs3739232 C G rs3739232 4.12E-06 Intracerebral hemorrhage HPOID:0001342 DOID:6713 C UTR-5 GWASdb_trait 8 142139187 rs3739231 C T rs3739231 4.56E-06 Intracerebral hemorrhage HPOID:0001342 DOID:6713 A intron GWASdb_trait 8 142139251 rs6578152 T C rs6578152 6.33E-06 Intracerebral hemorrhage HPOID:0001342 DOID:6713 C intron GWASdb_trait 8 142151713 rs307766 C T rs307766 6.60E-04 Alcohol dependence HPOID:0000707 DOID:0050741 A intron GWASdb_trait 8 142161064 rs3816063 C G,T rs3816063 2.00E-06 Obesity-related traits HPOID:0001513 DOID:9970 G intron GWASdb_trait 8 142198596 rs7001673 G T rs7001673 4.97E-09 Narcolepsy HPOID:0100786 DOID:8986 T intron GWASdb_trait 8 142198596 rs7001673 G T rs7001673 7.58E-04 Body mass index HPOID:0001507 DOID:9970 T intron GWASdb_trait 8 142198682 rs6988366 T C rs6988366 1.50E-05 Urinary metabolites HPOID:0000079 DOID:557 T intron GWASdb_trait 8 142198682 rs6988366 T C rs6988366 3.09E-04 Body mass index HPOID:0001507 DOID:9970 T intron GWASdb_trait 8 142198682 rs6988366 T C rs6988366 3.71E-04 Body mass index HPOID:0001507 DOID:9970 T intron GWASdb_trait 8 142201477 rs13270024 T C rs13270024 3.29E-04 Attention deficit hyperactivity disorder HPOID:0007018 DOID:1094 T intron GWASdb_trait 8 142205237 rs9792 A G rs9792 7.98E-04 Body mass index HPOID:0001507 DOID:9970 C UTR-3 GWASdb_trait