{{Rsnum
|rsid=2293370
|Gene=C3orf1
|Chromosome=3
|position=119501087
|Orientation=minus
|GMAF=0.2103
|Gene_s=TIMMDC1
|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 | 73.5 | 23.0 | 3.5
| HCB | 46.0 | 40.9 | 13.1
| JPT | 52.2 | 39.8 | 8.0
| YRI | 57.1 | 38.1 | 4.8
| ASW | 70.2 | 29.8 | 0.0
| CHB | 46.0 | 40.9 | 13.1
| CHD | 43.1 | 42.2 | 14.7
| GIH | 65.3 | 30.7 | 4.0
| LWK | 68.2 | 26.4 | 5.5
| MEX | 84.5 | 15.5 | 0.0
| MKK | 59.6 | 36.5 | 3.8
| TSI | 60.8 | 34.3 | 4.9
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21399635
|Trait=None
|Title=Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis
|RiskAllele=G
|Pval=3E-11
|OR=1.3500
|ORtxt=[1.23-1.47]
|OA=1
}}

{{PMID Auto GWAS
  |PMID=23000144
  |Trait=Primary biliary cirrhosis
  |Title=Genome-wide association study identifies TNFSF15 and POU2AF1 as susceptibility loci for primary biliary cirrhosis in the Japanese population.
  |RiskAllele=C
  |Pval=3E-9
  |OR=1.48
  |ORtxt=[1.29-1.68]
  |OA=1
}}

{{PMID Auto GWAS
  |PMID=21833088
  |Trait=Multiple sclerosis
  |Title=Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
  |RiskAllele=G
  |Pval=3E-9
  |OR=1.13
  |ORtxt=[1.11-1.15]
  |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}}