{{Rsnum
|rsid=2697962
|Gene=PRDM2
|Chromosome=1
|position=13824497
|Orientation=minus
|GMAF=0.1561
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=PRDM2
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.9 | 24.8 | 74.3
| HCB | 2.9 | 27.7 | 69.3
| JPT | 8.0 | 40.2 | 51.8
| YRI | 2.7 | 19.7 | 77.6
| ASW | 1.8 | 17.9 | 80.4
| CHB | 2.9 | 27.7 | 69.3
| CHD | 2.8 | 31.2 | 66.1
| GIH | 5.0 | 52.5 | 42.6
| LWK | 4.5 | 21.8 | 73.6
| MEX | 1.8 | 33.3 | 64.9
| MKK | 1.3 | 27.1 | 71.6
| TSI | 3.9 | 25.5 | 70.6
| HapMapRevision=28
}}

{{Report GE
|PubMed=16252231
|Source=pubmed
|AffyProbeset=SNP_A-8401263
|AffyOrientation=reverse
|AlleleA=C
|AlleleB=T
|onGW5=
|rsid=2697962
|ancestral=A
|RiskPopulation=
|RiskAllele=A
|CaseFreq=
|ControlFreq=
|OddsRatioHet=
|OddsRatioHom=
|OddsRatioAll=1.67
|Disease=Parkinson's disease
|DiseaseSymbol=PKD
|OA=1
}}

rs2697962 is in linkage disequilibrium with a polymorphism that increases susceptibility to Parkinson's disease 1.67 times for carriers of the A allele {{PMID|16252231|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 | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}