{{Rsnum
|rsid=397515620
|Chromosome=X
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=BCAP31
|position=153720968
|Gene_s=BCAP31
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=X
|CLNACC=RCV000059316.11
|CLNALLE=1
|CLNDBN=Chromosome Xq28 deletion syndrome
|CLNDSDB=MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=C1845408:300475:369939:369942
|CLNHGVS=NC_000023.10:g.152986423G>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=300398.0003
|Disease=Chromosome Xq28 deletion syndrome
|FwdALT=T
|FwdREF=C
|GENEINFO=BCAP31:10134
|GENE_ID=10134
|GENE_NAME=BCAP31
|REF=G
|RSPOS=152986423
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=397515620
}}