{{Rsnum
|rsid=376393123
|Chromosome=3
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=CTNNB1
|position=41225850
|Gene_s=CTNNB1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G,T
|CHROM=3
|CLNACC=RCV000032860.26
|CLNALLE=2
|CLNDBN=Mental retardation, autosomal dominant 19
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=CN165603:615075
|CLNHGVS=NC_000003.11:g.41267341C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=116806.0019
|Disease=Mental retardation
|FwdALT=G,T
|FwdREF=C
|GENEINFO=CTNNB1:1499
|GENE_ID=1499
|GENE_NAME=CTNNB1
|REF=C
|RSPOS=41267341
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;S3D;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=376393123
}}