{{Rsnum
|rsid=397514554
|Chromosome=3
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CTNNB1
|position=41234157
|Gene_s=CTNNB1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=3
|CLNACC=RCV000032859.22
|CLNALLE=1
|CLNDBN=Mental retardation, autosomal dominant 19
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=CN165603:615075
|CLNHGVS=NC_000003.11:g.41275648C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=116806.0018
|Disease=Mental retardation
|FwdALT=T
|FwdREF=C
|GENEINFO=CTNNB1:1499
|GENE_ID=1499
|GENE_NAME=CTNNB1
|REF=C
|RSPOS=41275648
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=397514554
}}