{{Rsnum
|rsid=4130047
|Gene=RIT2
|Chromosome=18
|position=43098270
|Orientation=plus
|GMAF=0.3301
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=RIT2
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 12.4 | 44.2 | 43.4
| HCB | 16.8 | 51.8 | 31.4
| JPT | 10.6 | 42.5 | 46.9
| YRI | 5.4 | 36.7 | 57.8
| ASW | 14.0 | 29.8 | 56.1
| CHB | 16.8 | 51.8 | 31.4
| CHD | 16.7 | 47.2 | 36.1
| GIH | 9.9 | 41.6 | 48.5
| LWK | 6.4 | 43.1 | 50.5
| MEX | 12.1 | 44.8 | 43.1
| MKK | 16.0 | 50.0 | 34.0
| TSI | 8.8 | 47.1 | 44.1
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21738487
|Trait=None
|Title=Web-based genome-wide association study identifies two novel Loci and a substantial genetic component for Parkinson's disease.
|RiskAllele=C
|Pval=2E-7
|OR=1.1600
|ORtxt=[1.10-1.23]
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}