{{Rsnum
|rsid=1860545
|Gene=TNFRSF1A
|Chromosome=12
|position=6337611
|Orientation=minus
|GMAF=0.2475
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=TNFRSF1A
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 29.2 | 47.8 | 23.0
| HCB | 80.3 | 19.0 | 0.7
| JPT | 66.4 | 31.0 | 2.7
| YRI | 90.5 | 9.5 | 0.0
| ASW | 80.7 | 19.3 | 0.0
| CHB | 80.3 | 19.0 | 0.7
| CHD | 79.8 | 18.3 | 1.8
| GIH | 48.5 | 41.6 | 9.9
| LWK | 89.1 | 10.9 | 0.0
| MEX | 51.8 | 37.5 | 10.7
| MKK | 69.7 | 26.5 | 3.9
| TSI | 36.3 | 45.1 | 18.6
| HapMapRevision=28
}}{{PMID Auto
|PMID=20430450
|Title=Validation of the CD6 and TNFRSF1A loci as risk factors for multiple sclerosis in Spain
}}

{{PMID Auto
|PMID=18520591
|Title=Sequence variants in host cell factor C1 are associated with Meniere's disease.
|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 | Illumina Human 1M}}