Disease associated variation - ClinVar Allele ID Type Name RS#dbSNP Phenotype IDs Chromosome Start Stop Reference Alternate 360516 single nucleotide variant NM_001184742.1(ZBTB33):c.37C>G (p.Gln13Glu) 1057518570 MedGen:CN169374 X 120253452 120253452 C G 360516 single nucleotide variant NM_001184742.1(ZBTB33):c.37C>G (p.Gln13Glu) 1057518570 MedGen:CN169374 X 119387307 119387307 C G

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 rs7882480 X 119389966 119389966 UTR3 0.55681 0.254292973638478

Disease associated variation - OMIM Ensembl_gene_ID Approved Gene Symbol MIM Number ENSG00000177485.6 ZBTB33 300329