PIAS4
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
194013389rs7257356CTrs72573567.34E-05NephrolithiasisHPOID:0000787DOID:585CintronGWASdb_trait
194014065rs8113562GArs81135625.12E-05NephrolithiasisHPOID:0000787DOID:585AintronGWASdb_trait
194020370rs12982708CTrs129827081.53E-05Word readingHPOID:0010522|HPOID:0100543|HPOID:0002463DOID:92|DOID:93|DOID:1561|DOID:13365CintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000105229.6 PIAS4 605989