{{Rsnum
|rsid=397509413
|Chromosome=3
|position=52409597
|Orientation=minus
|geno1=(-;-)
|geno2=(-;GG)
|geno3=(GG;GG)
|Gene=BAP1
|Gene_s=BAP1,PHF7
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=3
|CLNACC=RCV000049289.2
|CLNALLE=1
|CLNDBN=Tumor predisposition syndrome
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C3280492:614327:289539
|CLNHGVS=NC_000003.11:g.52443613_52443614delCC
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=603089.0010
|Disease=Tumor predisposition syndrome
|FwdREF=GG
|REF=ACC
|RSPOS=52443612
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050060000000000002110200
|WGT=0
|dbSNPBuildID=136
|rsid=397509413
|GENEINFO=PHF7:51533; BAP1:8314
|GENE_ID=51533; 8314
|GENE_NAME=PHF7; BAP1
}}