{{Rsnum
|rsid=6659742
|Gene=C1orf204
|Chromosome=1
|position=159848723
|Orientation=plus
|GMAF=0.3691
|Gene_s=C1orf204
|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 | 41.6 | 45.1 | 13.3
| HCB | 57.7 | 38.0 | 4.4
| JPT | 55.8 | 37.2 | 7.1
| YRI | 38.8 | 49.0 | 12.2
| ASW | 40.4 | 49.1 | 10.5
| CHB | 57.7 | 38.0 | 4.4
| CHD | 55.0 | 39.4 | 5.5
| GIH | 35.6 | 55.4 | 8.9
| LWK | 41.8 | 47.3 | 10.9
| MEX | 29.3 | 41.4 | 29.3
| MKK | 46.2 | 46.2 | 7.7
| TSI | 35.3 | 50.0 | 14.7
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23472185
  |Trait=Multiple sclerosis (OCB status)
  |Title=Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles.
  |RiskAllele=
  |Pval=7E-7
  |OR=1.99
  |ORtxt=[1.52-2.61]
  |OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}