WDR17
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
4176993039rs1385614TCrs13856144.60E-05Parent of origin effect on language impairment (paternal)HPOID:0002463DOID:93CintronGWASdb_trait
4177025984rs7698815AGrs76988153.22E-04Birth weightHPOID:0004323DOID:783|DOID:9352|DOID:1287GintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000150627.15 WDR17 609005