Disease associated variation - ClinVar Allele ID Type Name RS#dbSNP Phenotype IDs Chromosome Start Stop Reference Alternate 226641 single nucleotide variant NM_001198956.1(DCAF6):c.2240G>A (p.Arg747Gln) 145189179 MedGen:CN235864 1 168014447 168014447 G A 226641 single nucleotide variant NM_001198956.1(DCAF6):c.2240G>A (p.Arg747Gln) 145189179 MedGen:CN235864 1 168045209 168045209 G A

Disease associated variation - GWAS Central Study Name Source Marker Accession Chromosome Marker Start Marker Stop Alleles Gene Section P-value -log(p-value) GWAS of prostate cancer rs10489206 1 168041232 168041232 intronic 0.735649 0.133329351047778 GWAS of prostate cancer rs202248 1 167972023 167972023 intronic 0.50392 0.297638404658184 GWAS of prostate cancer rs12059592 1 167944643 167944643 intronic 0.17844 0.748507785430421

Disease associated variation - OMIM Ensembl_gene_ID Approved Gene Symbol MIM Number ENSG00000143164.15 DCAF6 610494