{{Rsnum
|rsid=17011455
|Gene=FAM176A
|Chromosome=2
|position=75563363
|Orientation=plus
|GMAF=0.06107
|Gene_s=FAM176A
|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 | 0.9 | 0.9 | 98.2
| HCB | 0.7 | 16.1 | 83.2
| JPT | 0.0 | 15.9 | 84.1
| YRI | 0.7 | 18.1 | 81.2
| ASW | 3.6 | 19.6 | 76.8
| CHB | 0.7 | 16.1 | 83.2
| CHD | 0.0 | 10.1 | 89.9
| GIH | 0.0 | 7.9 | 92.1
| LWK | 2.8 | 22.9 | 74.3
| MEX | 0.0 | 0.0 | 0.0
| MKK | 4.5 | 25.6 | 69.9
| TSI | 0.0 | 2.9 | 97.1
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23509613
  |Trait=Presence of antiphospholipid antibodies
  |Title=Genome-wide association study of antiphospholipid antibodies.
  |RiskAllele=
  |Pval=5E-6
  |OR=5.21
  |ORtxt=[NR]
  |OA=1
}}

{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}