{{Rsnum
|rsid=4075958
|Gene=RGS14
|Chromosome=5
|position=177357511
|Orientation=plus
|GMAF=0.1974
|Gene_s=RGS14
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 10.7 | 40.2 | 49.1
| HCB | 3.0 | 28.9 | 68.1
| JPT | 3.6 | 34.2 | 62.2
| YRI | 0.0 | 12.5 | 87.5
| ASW | 1.8 | 19.3 | 78.9
| CHB | 3.0 | 28.9 | 68.1
| CHD | 2.8 | 21.5 | 75.7
| GIH | 4.0 | 39.6 | 56.4
| LWK | 0.0 | 10.2 | 89.8
| MEX | 8.8 | 33.3 | 57.9
| MKK | 3.2 | 22.4 | 74.4
| TSI | 8.8 | 35.3 | 55.9
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21833088
|Trait=None
|Title=Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
|RiskAllele=A
|Pval=5E-7
|OR=1.0900
|ORtxt=[1.08-1.11]
|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}}