COPB2
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
3139091219rs9859864GTrs98598646.13E-05Schizophrenia(age at onset)HPOID:0100753DOID:5419TintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000184432.9 COPB2 606990