{{Rsnum
|rsid=121434543
|Chromosome=16
|Orientation=plus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=CDH3
|position=68681065
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CDH3
}}{{omim
|id=114021
|rsnum=121434543
|variant=0003
}}{{ClinVar
|rsid=121434543
|Reversed=0
|FwdREF=A
|FwdALT=T
|REF=A
|ALT=T
|RSPOS=68714968
|CHROM=16
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=CDH3:1001
|GENE_NAME=CDH3
|GENE_ID=1001
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.68714968A>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=114021.0003
|CLNSIG=5
|CLNCUI=C1857041
|CLNDBN=EEM syndrome
|Disease=EEM syndrome
|CLNACC=RCV000019207.26
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1857041:225280:1897
}}