{{Rsnum
|rsid=398122907
|Chromosome=3
|Orientation=plus
|geno1=(-;-)
|geno2=(-;TTCT)
|geno3=(TTCT;TTCT)
|Gene=CTNNB1
|position=41233615
|Gene_s=CTNNB1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=3
|CLNACC=RCV000032858.27
|CLNALLE=1
|CLNDBN=Mental retardation, autosomal dominant 19
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=CN165603:615075
|CLNHGVS=NC_000003.11:g.41275106_41275109delTTCT
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=116806.0017
|Disease=Mental retardation
|FwdREF=TTCT
|GENEINFO=CTNNB1:1499
|GENE_ID=1499
|GENE_NAME=CTNNB1
|REF=ATTCT
|RSPOS=41275101
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050060000000000002110200
|WGT=0
|dbSNPBuildID=138
|rsid=398122907
}}