RNF14
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
5141354220rs187542GCrs1875424.99E-06Lymphocyte countsHPOID:0004332|HPOID:0002665DOID:2841|DOID:1240|DOID:0060058|DOID:614|DOID:1287GintronGWASdb_trait
5141362162rs252095AGrs2520954.58E-05Amyotrophic Lateral SclerosisHPOID:0007354DOID:332CintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000013561.17 RNF14 605675