{{Rsnum
|rsid=351771
|Gene=APC
|Chromosome=5
|position=112828864
|Orientation=plus
|GMAF=0.3393
|Gene_s=APC
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 8.0 | 55.8 | 36.3
| HCB | 2.2 | 32.6 | 65.2
| JPT | 1.8 | 25.0 | 73.2
| YRI | 25.0 | 49.3 | 25.7
| ASW | 21.4 | 46.4 | 32.1
| CHB | 2.2 | 32.6 | 65.2
| CHD | 7.3 | 35.8 | 56.9
| GIH | 3.0 | 39.0 | 58.0
| LWK | 21.1 | 51.4 | 27.5
| MEX | 6.9 | 34.5 | 58.6
| MKK | 19.2 | 51.3 | 29.5
| TSI | 21.8 | 44.6 | 33.7
| HapMapRevision=28
}}{{PMID Auto
|PMID=24078348
|Title=An Analysis of Polymorphisms Within the Wnt Signaling Pathway in Relation to Ovarian Cancer Risk in a Polish Population
|OA=1
}}

{{PMID Auto
|PMID=16569251
|Title=Single nucleotide polymorphisms of the APC gene and colorectal cancer risk: a case-control study in Taiwan.
|OA=1
}}

{{PMID Auto
|PMID=18849522
|Title=Nested Patch PCR enables highly multiplexed mutation discovery in candidate genes.
|OA=1
}}

{{PMID Auto
|PMID=20333795
|Title=APC gene mutations in Chinese familial adenomatous polyposis patients.
|OA=1
}}

{{ClinVar
|ALT=A
|CAF=0.3393; 0.6607
|CHROM=5
|CLNACC=RCV000035066.2; RCV000074153.1
|CLNALLE=1
|CLNDBN=AllHighlyPenetrant; Familial colorectal cancer
|CLNDSDB=MedGen; GeneReviews:MedGen:OMIM
|CLNDSDBID=CN169374; NBK1211:CN029768:114500
|CLNHGVS=NC_000005.9:g.112164561G>A
|CLNORIGIN=0
|CLNSIG=255
|CLNSRC=Emory University
|CLNSRCID=2626
|COMMON=1
|Disease=AllHighlyPenetrant; Familial colorectal cancer
|FwdALT=T
|FwdREF=C
|GENEINFO=APC:324
|GENE_ID=324
|GENE_NAME=APC
|REF=G
|RSPOS=112164561
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;S3D;SLO;VLD;G5A;G5;HD;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;PH3;LSD;OM
|VC=SNV
|VP=0x05036800000017051f110100
|WGT=0
|dbSNPBuildID=79
|rsid=351771
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}