{{Rsnum
|rsid=6963573
|Chromosome=7
|position=36788795
|Orientation=plus
|GMAF=0.07713
|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 | 0.9 | 28.3 | 70.8
| HCB | 0.0 | 0.7 | 99.3
| JPT | 0.0 | 0.0 | 100.0
| YRI | 0.0 | 9.5 | 90.5
| ASW | 3.5 | 8.8 | 87.7
| CHB | 0.0 | 0.7 | 99.3
| CHD | 0.0 | 0.9 | 99.1
| GIH | 5.0 | 35.6 | 59.4
| LWK | 0.9 | 15.5 | 83.6
| MEX | 0.0 | 13.8 | 86.2
| MKK | 0.6 | 15.4 | 84.0
| TSI | 2.0 | 22.5 | 75.5
| HapMapRevision=28
}}

{{Report GE
|PubMed=16252231
|Source=pubmed
|AffyProbeset=SNP_A-2183433
|AffyOrientation=reverse
|AlleleA=C
|AlleleB=T
|onGW5=
|rsid=6963573
|ancestral=G
|RiskPopulation=
|RiskAllele=A
|CaseFreq=
|ControlFreq=
|OddsRatioHet=
|OddsRatioHom=
|OddsRatioAll=1.71
|Disease=Parkinson's disease
|DiseaseSymbol=PKD
|OA=1
}}

rs6963573 is in linkage disequilibrium with a polymorphism that increases susceptibility to Parkinson's disease 1.71 times for carriers of the A allele {{PMID|16252231|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | Affy500k}}
{{on chip | HumanOmni1Quad}}