RNF32
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
7156442203rs4716438TCrs47164384.02E-08Lymphocyte countsHPOID:0004332|HPOID:0002665DOID:2841|DOID:1240|DOID:0060058|DOID:614|DOID:1287CintronGWASdb_trait
7156447708rs2108794GArs21087941.41E-04Smoking quantityHPOID:0000707DOID:0050742CintronGWASdb_trait
7156468559rs3823617TCrs38236173.62E-04Acute lung injuryHPOID:0002088DOID:850Asplice-5GWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000105982.16 RNF32 610241