{{Rsnum
|rsid=2233287
|Gene=TNIP1
|Chromosome=5
|position=151060536
|Orientation=minus
|GMAF=0.09688
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=TNIP1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 89.4 | 9.7 | 0.9
| HCB | 100.0 | 0.0 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 61.9 | 33.3 | 4.8
| ASW | 56.1 | 36.8 | 7.0
| CHB | 100.0 | 0.0 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 92.1 | 7.9 | 0.0
| LWK | 63.6 | 33.6 | 2.7
| MEX | 75.9 | 24.1 | 0.0
| MKK | 73.1 | 25.0 | 1.9
| TSI | 83.3 | 16.7 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21750679
|Trait=None
|Title=Genome-wide scan identifies TNIP1, PSORS1C1, and RHOB as novel risk loci for systemic sclerosis.
|RiskAllele=A
|Pval=5E-9
|OR=1.3100
|ORtxt=[1.15-1.43]
|OA=1
}}

{{PMID Auto
|PMID=20159110
|Title=Allelic skewing of DNA methylation is widespread across the genome.
|OA=1
}}

{{PMID Auto
|PMID=22896740
|Title=Confirmation of TNIP1 but not RHOB and PSORS1C1 as systemic sclerosis risk factors in a large independent replication study
|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}}