DCAF5
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
1469604244rs8008735ACrs80087358.66E-04Amyotrophic lateral sclerosis (sporadic)HPOID:0007354DOID:332AintronGWASdb_trait
1469619173rs1275419ACrs12754199.77E-05Coronary heart diseaseHPOID:0001677DOID:3393CintronGWASdb_trait
Disease associated variation - OMIM
Ensembl_gene_ID Approved Gene Symbol MIM Number
ENSG00000139990.17 DCAF5 603812