{{Rsnum
|rsid=719725
|Chromosome=9
|position=6365683
|Orientation=plus
|GMAF=0.3255
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=131
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}
{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 36.9 | 44.6 | 18.5
| HCB | 64.4 | 26.7 | 8.9
| JPT | 45.5 | 45.5 | 9.1
| YRI | 49.2 | 42.9 | 7.9
| ASW | 0.0 | 0.0 | 0.0
| CHB | 64.4 | 26.7 | 8.9
| 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
}}[[rs719725]] is a SNP on chromosome 9p24 that has been associated with increased risk of [[colorectal cancer]], based on a study of 1,567 sibships from the Colon Cancer Family Registry.

By genotypes, the observed risks were as follows: (A;A) versus (C;C): odds ratios, 1.46, CI: 1.06-2.02; (A;C) versus (C;C): odds ratio 1.50, CI: 1.14-1.98; p = 0.011){{PMID|18056436}}

{{PMID Auto
|PMID=20978172
|Title=Characterization of 9p24 risk locus and colorectal adenoma and cancer: gene-environment interaction and meta-analysis
|OA=1
}} : gave an overall meta-analysis (n=17) OR of 1.07 (95% CI 1.03-1.12, p-trend 0.001).
{{PMID Auto
|PMID=21102338
|Title=Possible association between a genetic polymorphism at 8q24 and risk of upper gastrointestinal cancer
|OA=1
}}
{{PMID Auto
|PMID=21119214
|Title=Colorectal Cancer Susceptibility Loci in a Population-Based Study: Associations with Morphological Parameters
|OA=1
}}

{{PMID Auto
|PMID=21952639
|Title=NIRF constitutes a nodal point in the cell cycle network and is a candidate tumor suppressor
|OA=1
}}

{{PMID Auto
|PMID=19155440
|Title=Meta association of colorectal cancer confirms risk alleles at 8q24 and 18q21.
|OA=1
}}

{{PMID Auto
|PMID=20648012
|Title=Association studies on 11 published colorectal cancer risk loci.
|OA=1
}}

{{PMID Auto
|PMID=21071539
|Title=Generalizability and epidemiologic characterization of eleven colorectal cancer GWAS hits in multiple populations.
|OA=1
}}

{{PMID Auto
|PMID=23359760
|Title=Single-nucleotide polymorphism associations for colorectal cancer in southern chinese population
|OA=1
}}

{{PMID Auto
|PMID=22848671
|Title=Association of eleven common, low-penetrance colorectal cancer susceptibility genetic variants at six risk loci with clinical outcome.
|OA=1
}}

{{PMID Auto
|PMID=23434150
|Title=Are the common genetic variants associated with colorectal cancer risk for DNA mismatch repair gene mutation carriers?
|OA=1
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}