FEM1C
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
5114866191rs256940GArs2569403.84E-05Educational attainmentHPOID:0000118NAAintronGWASdb_trait
5114877920rs256957AGrs2569573.30E-05C-Reactive ProteinHPOID:0010876DOID:14221|DOID:9352|DOID:10763|DOID:5844GintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000145780.7 FEM1C 608767