{{Rsnum
|rsid=1569723
|Chromosome=20
|position=46113425
|Orientation=plus
|GMAF=0.2443
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 55.8 | 40.7 | 3.5
| HCB | 45.6 | 44.9 | 9.6
| JPT | 29.2 | 51.3 | 19.5
| YRI | 98.6 | 1.4 | 0.0
| ASW | 96.5 | 3.5 | 0.0
| CHB | 45.6 | 44.9 | 9.6
| CHD | 43.0 | 41.1 | 15.9
| GIH | 53.5 | 39.6 | 6.9
| LWK | 93.6 | 6.4 | 0.0
| MEX | 53.4 | 39.7 | 6.9
| MKK | 85.7 | 13.6 | 0.6
| TSI | 42.2 | 55.9 | 2.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=19525955
|Title=Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20
}}

{{omim
|id=126200
|rsnum=1569723
}}

{{PMID Auto GWAS
|PMID=22446961
|Trait=None
|Title=Two new susceptibility loci for Kawasaki disease identified through genome-wide association analysis.
|RiskAllele=A
|Pval=6E-9
|OR=1.4150
|ORtxt=None
}}

{{PMID|20018027|OA=1
}} Conditional analysis of the major histocompatibility complex in rheumatoid arthritis.

{{PMID|20018074|OA=1
}} Identifying rheumatoid arthritis susceptibility genes using high-dimensional methods.

{{PMID|20405052|OA=1
}} The effect of single nucleotide polymorphisms from genome wide association studies in multiple sclerosis on gene expression.

{{PMID Auto GWAS
  |PMID=23128233
  |Trait=Inflammatory bowel disease
  |Title=Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.
  |RiskAllele=C
  |Pval=1E-13
  |OR=1.09
  |ORtxt=[1.056-1.126]
  |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 | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}