{{Rsnum
|rsid=6457620
|Chromosome=6
|position=32696222
|Orientation=plus
|GMAF=0.4389
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 26.5 | 51.3 | 22.1
| HCB | 29.9 | 46.0 | 24.1
| JPT | 38.1 | 46.9 | 15.0
| YRI | 18.4 | 51.0 | 30.6
| ASW | 38.6 | 35.1 | 26.3
| CHB | 29.9 | 46.0 | 24.1
| CHD | 28.4 | 57.8 | 13.8
| GIH | 17.8 | 57.4 | 24.8
| LWK | 33.0 | 50.5 | 16.5
| MEX | 51.7 | 41.4 | 6.9
| MKK | 22.4 | 50.0 | 27.6
| TSI | 30.4 | 50.0 | 19.6
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=18794853
|Trait=Rheumatoid arthritis
|Title=Common variants at CD40 and other loci confer risk of rheumatoid arthritis
|RiskAllele=
|Pval=0
|OR=2.55
|ORtxt=[2.40-2.71]
|OA=1
}}

An [[ambiguous flip]] whose risk allele could not be determined from the original data {{doi|10.1371/journal.pone.0023473}}  

{{PMID|17660530}} Risk alleles for multiple sclerosis identified by a genomewide study.

{{PMID|20335276|OA=1
}} PheWAS: demonstrating the feasibility of a phenome-wide scan to discover gene-disease associations.

{{PMID|20369022|OA=1
}} Candidate causal regulatory effects by integration of expression QTLs with complex trait genetic associations.

{{PMID|20426808|OA=1
}} AntEpiSeeker: detecting epistatic interactions for case-control studies using a two-stage ant colony optimization algorithm.

{{PMID|20546594|OA=1
}} An application of Random Forests to a genome-wide association dataset: methodological considerations & new findings.

{{PMID|21739420}} Genetic variants in the HLA-DRB1 gene are associated with Kashin-Beck disease in the Tibetan population.

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs6457620
|overall_frequency_n=64
|overall_frequency_d=116
|overall_frequency=0.551724
|n_genomes=37
|n_genomes_annotated=0
|n_haplomes=52
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=2
|webscore=N
}}

{{PMID Auto GWAS
  |PMID=20881960
  |Trait=Height
  |Title=Hundreds of variants clustered in genomic loci and biological pathways affect human height.
  |RiskAllele=C
  |Pval=2E-16
  |OR=.03
  |ORtxt=[NR] unit decrease
  |OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}