View source for Rs4645843

{{Rsnum
|rsid=4645843
|StabilizedOrientation=plus
|Chromosome=6
|position=31576785
|Gene_s=TNF
|Gene=TNF
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Assembly=GRCh38.p7
|GenomeBuild=38.3
|dbSNPBuild=150
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 99.1 | 0.9 | 0.0
| HCB | 100.0 | 0.0 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 100.0 | 0.0 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 100.0 | 0.0 | 0.0
| CHD | 99.1 | 0.9 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 99.1 | 0.9 | 0.0
| MEX | 98.2 | 1.8 | 0.0
| MKK | 99.4 | 0.6 | 0.0
| TSI | 98.0 | 2.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=28993561
|Title=A Missense Variant rs4645843 in TNF-α Gene Is a Risk Factor of Polycystic Ovary Syndrome in the Uygur Population.
}}
{{on chip | 23andMe v3}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}
{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | FTDNA}}
{{on chip | FTDNA2}}
{{on chip | 23andMe v4}}
{{on chip | Ancestry v2}}
{{on chip | Ancestry v2c}}
{{on chip | Ancestry v2d}}