{{Rsnum
|rsid=3792783
|Gene=TNIP1
|Chromosome=5
|position=151076171
|Orientation=minus
|GMAF=0.258
|Gene_s=TNIP1
|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 | 1.8 | 24.8 | 73.5
| HCB | 4.4 | 31.4 | 64.2
| JPT | 2.7 | 35.4 | 61.9
| YRI | 32.7 | 49.0 | 18.4
| ASW | 14.0 | 49.1 | 36.8
| CHB | 4.4 | 31.4 | 64.2
| CHD | 3.7 | 32.1 | 64.2
| GIH | 3.0 | 35.6 | 61.4
| LWK | 26.4 | 59.1 | 14.5
| MEX | 0.0 | 31.0 | 69.0
| MKK | 14.7 | 48.1 | 37.2
| TSI | 2.0 | 24.5 | 73.5
| HapMapRevision=28
}}{{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
}}

{{PMID Auto
|PMID=23944604
|Title=Association of genes in the NF-κB pathway with antibody-positive primary Sjögren's syndrome
}}

{{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}}