{{Rsnum
|rsid=11954856
|Gene=APC
|Chromosome=5
|position=112751630
|Orientation=plus
|GMAF=0.3898
|Gene_s=APC
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 21.9 | 67.2 | 10.9
| HCB | 68.2 | 29.5 | 2.3
| JPT | 68.2 | 29.5 | 2.3
| YRI | 22.6 | 48.4 | 29.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 68.2 | 29.5 | 2.3
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| 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=18708403
|Title=Association of genetic variation in genes implicated in the beta-catenin destruction complex with risk of breast cancer.
|OA=1
}}

{{ClinVar
|ALT=G
|CAF=0.3898; 0.6102
|CHROM=5
|CLNACC=RCV000073790.1
|CLNALLE=1
|CLNDBN=Familial colorectal cancer
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1211:CN029768:114500
|CLNHGVS=NC_000005.9:g.112087327T>G
|CLNORIGIN=0
|CLNSIG=255
|COMMON=1
|Disease=Familial colorectal cancer
|FwdALT=G
|FwdREF=T
|GENEINFO=APC:324
|GENE_ID=324
|GENE_NAME=APC
|REF=T
|RSPOS=112087327
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;SLO;VLD;G5A;G5;HD;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;PH3;LSD;OM
|VC=SNV
|VP=0x05016800000017051f110100
|WGT=0
|dbSNPBuildID=120
|rsid=11954856
}}

{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}