{{Rsnum
|rsid=121434618
|Chromosome=X
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=BCOR
|position=40075092
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=BCOR
}}{{omim
|id=300485
|rsnum=121434618
|variant=0001
}}{{ClinVar
|rsid=121434618
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=39934345
|CHROM=X
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=BCOR:54880
|GENE_NAME=BCOR
|GENE_ID=54880
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.39934345G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300485.0001
|CLNSIG=5
|CLNCUI=C1846265
|CLNDBN=Oculofaciocardiodental syndrome
|Disease=Oculofaciocardiodental syndrome
|CLNACC=RCV000011658.5
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1521:C1846265:300166:2712:568
}}