{{Rsnum
|rsid=16865717
|Gene=RSAD2
|Chromosome=2
|position=6892487
|Orientation=plus
|GMAF=0.3287
|Gene_s=RSAD2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 57.5 | 37.2 | 5.3
| HCB | 64.2 | 32.1 | 3.6
| JPT | 63.7 | 31.9 | 4.4
| YRI | 22.4 | 49.0 | 28.6
| ASW | 12.3 | 49.1 | 38.6
| CHB | 64.2 | 32.1 | 3.6
| CHD | 65.1 | 32.1 | 2.8
| GIH | 36.6 | 46.5 | 16.8
| LWK | 20.0 | 52.7 | 27.3
| MEX | 55.2 | 36.2 | 8.6
| MKK | 25.0 | 54.5 | 20.5
| TSI | 48.0 | 41.2 | 10.8
| 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=9E-9
  |OR=1.56
  |ORtxt=[NR]
  |OA=1
}}

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