Disease associated variation - ClinVar Allele ID Type Name RS#dbSNP Phenotype IDs Chromosome Start Stop Reference Alternate 74424 copy number gain GRCh38/hg38 Xp21.2(chrX:30783431-30834542)x2 -1 - X 30801548 30852659 na na 74424 copy number gain GRCh38/hg38 Xp21.2(chrX:30783431-30834542)x2 -1 - X 30783431 30834542 na na 74424 copy number gain GRCh38/hg38 Xp21.2(chrX:30783431-30834542)x2 -1 - X 30711469 30762580 na na

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 rs5927631 X 30876844 30876844 intronic 0.628694 0.20156068436004898

Disease associated variation - OMIM Ensembl_gene_ID Approved Gene Symbol MIM Number ENSG00000157625.15 TAB3 300480