{{Rsnum
|rsid=10318
|Gene=GREM1
|Chromosome=15
|position=32733778
|Orientation=plus
|GMAF=0.2351
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=GREM1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 66.1 | 29.4 | 4.6
| HCB | 20.5 | 50.0 | 29.5
| JPT | 18.2 | 51.8 | 30.0
| YRI | 98.6 | 1.4 | 0.0
| ASW | 91.2 | 8.8 | 0.0
| CHB | 20.5 | 50.0 | 29.5
| CHD | 15.1 | 55.7 | 29.2
| GIH | 51.0 | 39.0 | 10.0
| LWK | 93.6 | 6.4 | 0.0
| MEX | 64.3 | 32.1 | 3.6
| MKK | 90.3 | 9.0 | 0.6
| TSI | 54.0 | 43.0 | 3.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=20659471
|Title=Genetic Heterogeneity in Colorectal Cancer Associations in Americans of African vs. European Descent
|OA=1
}}

{{PMID Auto
|PMID=21097774
|Title=Colorectal cancer susceptibility loci on chromosome 8q23.3 and 11q23.1 as modifiers for disease expression in lynch syndrome
}}

{{PMID Auto
|PMID=22505654
|Title=GWAS-identified colorectal cancer susceptibility loci associated with clinical outcomes
}}

{{PMID Auto
|PMID=19011631
|Title=Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer.
|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=24753543
|Title=Shared and Independent Colorectal Cancer Risk Alleles in TGFβ-related Genes in African and European Americans
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}