{{Rsnum
|rsid=6771316
|Gene=CEACAMP2
|Chromosome=3
|position=72091381
|Orientation=plus
|GMAF=0.112
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=LINC00877
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 1.8 | 31.0 | 67.3
| HCB | 1.5 | 22.8 | 75.7
| JPT | 0.0 | 13.3 | 86.7
| YRI | 1.4 | 20.4 | 78.2
| ASW | 0.0 | 26.3 | 73.7
| CHB | 1.5 | 22.8 | 75.7
| CHD | 1.9 | 18.5 | 79.6
| GIH | 1.0 | 18.8 | 80.2
| LWK | 0.9 | 20.0 | 79.1
| MEX | 0.0 | 3.4 | 96.6
| MKK | 0.6 | 14.2 | 85.2
| TSI | 1.0 | 21.6 | 77.5
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23509962
  |Trait=Venous thromboembolism (gene x gene interaction)
  |Title=A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.
  |RiskAllele=C
  |Pval=5E-9
  |OR=2.13
  |ORtxt=[NR]
  |OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | Illumina Human 1M}}