{{Rsnum
|rsid=1128977
|Gene=RXRG
|Chromosome=1
|position=165419892
|Orientation=minus
|GMAF=0.2392
|Gene_s=RXRG
|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 | 34.5 | 47.8 | 17.7
| HCB | 71.5 | 27.0 | 1.5
| JPT | 81.4 | 18.6 | 0.0
| YRI | 92.5 | 6.8 | 0.7
| ASW | 68.4 | 31.6 | 0.0
| CHB | 71.5 | 27.0 | 1.5
| CHD | 73.4 | 25.7 | 0.9
| GIH | 35.6 | 42.6 | 21.8
| LWK | 81.8 | 16.4 | 1.8
| MEX | 56.9 | 39.7 | 3.4
| MKK | 71.2 | 26.3 | 2.6
| TSI | 40.2 | 44.1 | 15.7
| HapMapRevision=28
}}

{{PMID Auto
|PMID=18937358
|Title=Characteristics of a spina bifida population including North American Caucasian and Hispanic individuals.
|OA=1
}}

{{PMID Auto
|PMID=24222859
|Title=Association of RXR-Gamma Gene Variants with Familial Combined Hyperlipidemia: Genotype and Haplotype Analysis
|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}}