{{Rsnum
|rsid=6932056
|Chromosome=6
|position=137921300
|Orientation=plus
|GMAF=0.03673
|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 | 0.0 | 4.4 | 95.6
| HCB | 0.0 | 11.7 | 88.3
| JPT | 2.7 | 14.2 | 83.2
| YRI | 0.0 | 8.8 | 91.2
| ASW | 0.0 | 7.0 | 93.0
| CHB | 0.0 | 11.7 | 88.3
| CHD | 0.0 | 12.0 | 88.0
| GIH | 1.0 | 8.9 | 90.1
| LWK | 0.0 | 6.4 | 93.6
| MEX | 0.0 | 3.4 | 96.6
| MKK | 1.9 | 17.3 | 80.8
| TSI | 0.0 | 6.9 | 93.1
| HapMapRevision=28
}}{{PMID Auto
|PMID=23124809
|Title=PLD4 as a novel susceptibility gene for systemic sclerosis in a Japanese population
}}

{{PMID Auto
|PMID=19387456
|Title=Meta-analysis and imputation identifies a 109 kb risk haplotype spanning TNFAIP3 associated with lupus nephritis and hematologic manifestations.
|OA=1
}}

{{PMID Auto
|PMID=19417005
|Title=Combined effects of three independent SNPs greatly increase the risk estimate for RA at 6q23.
|OA=1
}}

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