{{Rsnum
|rsid=137854580
|Chromosome=5
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=APC
|position=112827194
|Gene_s=APC
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=611731
|variant=0031
|rsnum=137854580
}}{{ClinVar
|rsid=137854580
|Reversed=0
|FwdREF=C
|FwdALT=G,T
|REF=C
|ALT=G,T
|RSPOS=112162891
|CHROM=5
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=APC:324
|GENE_NAME=APC
|GENE_ID=324
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000005.9:g.112162891C>G; NC_000005.9:g.112162891C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=611731.0031
|CLNSIG=5
|CLNCUI=C0017097
|CLNDBN=not provided; Gardner syndrome
|Disease=not provided; Gardner syndrome
|CLNACC=RCV000034403.1; RCV000000867.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:SNOMED_CT
|CLNDSDBID=C0017097:60876000
}}