AP1G2
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
1424033027rs12897422GArs128974221.00E-04Information processing speedHPOID:0100753|HPOID:0000716DOID:1561GmissenseGWASdb_trait
1424033070rs2281680CTrs22816806.00E-08Sudden cardiac arrestHPOID:0001645DOID:3393CintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000213983.11 AP1G2 603534