{{Rsnum
|rsid=2288073
|Gene=C2orf84
|Chromosome=2
|position=24190429
|Orientation=plus
|GMAF=0.2149
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=FAM228A
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 52.2 | 36.3 | 11.5
| HCB | 65.0 | 30.7 | 4.4
| JPT | 78.6 | 20.5 | 0.9
| YRI | 78.2 | 20.4 | 1.4
| ASW | 64.9 | 33.3 | 1.8
| CHB | 65.0 | 30.7 | 4.4
| CHD | 67.9 | 27.5 | 4.6
| GIH | 41.6 | 51.5 | 6.9
| LWK | 63.6 | 32.7 | 3.6
| MEX | 63.8 | 29.3 | 6.9
| MKK | 77.6 | 19.9 | 2.6
| TSI | 51.0 | 37.3 | 11.8
| 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=T
  |Pval=2E-9
  |OR=1.60
  |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 | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}