{{Rsnum
|rsid=615672
|Chromosome=6
|position=32606394
|Orientation=plus
|GMAF=0.4692
|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 | 1.5 | 30.8 | 67.7
| HCB | 42.2 | 46.7 | 11.1
| JPT | 33.3 | 40.0 | 26.7
| YRI | 27.0 | 49.2 | 23.8
| ASW | 0.0 | 0.0 | 0.0
| CHB | 42.2 | 46.7 | 11.1
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{Report GE
|PubMed=17554300
|Source=lit
|AffyProbeset=SNP_A-1956213
|AffyOrientation=same
|AlleleA=C
|AlleleB=G
|onGW5=1
|rsid=615672
|ancestral=G
|RiskPopulation=
|RiskAllele=
|CaseFreq=
|ControlFreq=
|OddsRatioHet=
|OddsRatioHom=
|OddsRatioAll=
|Disease=Rheumatoid Arthritis
|DiseaseSymbol=RA
|OA=1
}}

{{PMID|20017963|OA=1
}} Representation of genetic association via attributable familial relative risks in order to identify polymorphisms functionally relevant to rheumatoid arthritis.

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

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs615672
|overall_frequency_n=43
|overall_frequency_d=114
|overall_frequency=0.377193
|n_genomes=34
|n_genomes_annotated=0
|n_haplomes=37
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{PMID Auto
|PMID=23678157
|Title=Integrative analyses for functional mechanisms underlying associations for rheumatoid arthritis.
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | Affy GenomeWide 6}}
{{on chip | Affy500k}}
{{on chip | Illumina Human 1M}}