{{Rsnum
|rsid=13403289
|Chromosome=2
|position=179352004
|Orientation=plus
|GMAF=0.4922
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 29.2 | 56.6 | 14.2
| HCB | 34.3 | 46.0 | 19.7
| JPT | 36.3 | 49.6 | 14.2
| YRI | 2.0 | 21.8 | 76.2
| ASW | 3.5 | 40.4 | 56.1
| CHB | 34.3 | 46.0 | 19.7
| CHD | 29.4 | 52.3 | 18.3
| GIH | 35.6 | 46.5 | 17.8
| LWK | 4.5 | 39.1 | 56.4
| MEX | 34.5 | 46.6 | 19.0
| MKK | 9.6 | 48.7 | 41.7
| TSI | 41.2 | 41.2 | 17.6
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23509613
  |Trait=Presence of antiphospholipid antibodies
  |Title=Genome-wide association study of antiphospholipid antibodies.
  |RiskAllele=
  |Pval=6E-6
  |OR=2.42
  |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}}