TRIM6
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
115625603rs7108470AGrs71084703.00E-06IMMUNOGLOBULIN GGLYCOSYLTRANSFERASESIgG glycosylationHPOID:0010701DOID:2531|DOID:417GintronGWASdb_drug
115625603rs7108470AGrs71084703.00E-06IgG glycosylationHPOID:0010701DOID:2531|DOID:417GintronGWASdb_trait
115625988rs17304278TCrs173042784.58E-04Suicide attempts in bipolar disorderHPOID:0007302DOID:3312TintronGWASdb_trait
115626241rs1074353GArs10743533.13E-05Parent of origin effect on language impairment (maternal)HPOID:0002463DOID:93AintronGWASdb_trait
115630635rs4910828TCrs49108281.40E-05Calcium levelsHPOID:0004363|HPOID:0002621|HPOID:0011915DOID:10575|DOID:1936CintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000121236.20 TRIM6 607564