{{Rsnum
|rsid=11642873
|Chromosome=16
|position=85958099
|Orientation=plus
|GMAF=0.1189
|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 | 59.8 | 34.8 | 5.4
| HCB | 79.6 | 19.0 | 1.5
| JPT | 84.8 | 14.3 | 0.9
| YRI | 96.5 | 3.5 | 0.0
| ASW | 83.9 | 16.1 | 0.0
| CHB | 79.6 | 19.0 | 1.5
| CHD | 72.1 | 27.9 | 0.0
| GIH | 78.0 | 21.0 | 1.0
| LWK | 96.3 | 3.7 | 0.0
| MEX | 75.4 | 24.6 | 0.0
| MKK | 92.2 | 6.5 | 1.3
| TSI | 77.5 | 22.5 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21779181
|Trait=None
|Title=Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy.
|RiskAllele=
|Pval=2E-12
|OR=1.3300
|ORtxt=[1.23-1.45]
|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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}