{{Rsnum
|rsid=121913224
|Chromosome=5
|Orientation=plus
|geno1=(-;-)
|geno2=(-;AAAGA)
|geno3=(AAAGA;AAAGA)
|Gene=APC
|position=112839521
|Gene_s=APC
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=121913224
|Reversed=0
|FwdREF=AAAGA
|FwdALT=
|REF=AAAAGA
|ALT=A
|RSPOS=112175212
|CHROM=5
|dbSNPBuildID=133
|SSR=0
|SAO=3
|VP=0x050168000000000002110220
|GENEINFO=APC:324
|GENE_NAME=APC
|GENE_ID=324
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.112175218_112175222delAAAGA
|CLNSRC=GTR; GeneReviews; OMIM Allelic Variant
|CLNORIGIN=2
|CLNSRCID=GTR000330983; NBK1345; 611731.0023; 611731.0041
|CLNSIG=5
|CLNCUI=CN074282; CN074282; C0017097; C0017097; CN074282; CN074282
|CLNDBN=Adenomatous polyposis coli; Gardner syndrome; Adenomatous polyposis coli with congenital cholesteatoma; Familial multiple polyposis syndrome
|Disease=Adenomatous polyposis coli; Gardner syndrome; Adenomatous polyposis coli with congenital cholesteatoma; Familial multiple polyposis syndrome
|CLNACC=RCV000000856.1; RCV000000857.1; RCV000000858.1; RCV000035072.1
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT; MedGen:SNOMED_CT
|CLNDSDBID=NBK1345:CN074282:175100:220460:733:70921007; C0017097:60876000; C0032580:72900001
}}{{PMID Auto
|PMID=8162051
|Title=Regionally clustered APC mutations are associated with a severe phenotype and occur at a high frequency in new mutation cases of adenomatous polyposis coli.
}}

{{PMID Auto
|PMID=8281160
|Title=Identification of somatic APC gene mutations in periampullary adenomas in a patient with familial adenomatous polyposis (FAP).
}}

{{PMID Auto
|PMID=8929955
|Title=Familial adenomatous polyposis in a 5 year old child: a clinical, pathological, and molecular genetic study.
|OA=1
}}

{{PMID Auto
|PMID=9890479
|Title=Congenital cholesteatoma in a child carrying a gene mutation for adenomatous polyposis coli.
}}