{{Rsnum
|rsid=4837628
|Gene=DBC1
|Chromosome=9
|position=119297431
|Orientation=plus
|GMAF=0.4412
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=BRINP1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 23.0 | 49.6 | 27.4
| HCB | 9.5 | 45.3 | 45.3
| JPT | 15.0 | 43.4 | 41.6
| YRI | 34.0 | 44.9 | 21.1
| ASW | 42.1 | 47.4 | 10.5
| CHB | 9.5 | 45.3 | 45.3
| CHD | 6.4 | 53.2 | 40.4
| GIH | 11.9 | 51.5 | 36.6
| LWK | 41.8 | 49.1 | 9.1
| MEX | 15.5 | 46.6 | 37.9
| MKK | 33.8 | 52.6 | 13.6
| TSI | 14.7 | 48.0 | 37.3
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20070850
|Trait=Parkinson's disease
|Title=Genome-Wide Association Study Confirms SNPs in SNCA and the MAPT Region as Common Risk Factors for Parkinson Disease
|RiskAllele=A
|Pval=0.000001
|OR=1.27
|ORtxt=[1.15-1.39]
|OA=1
}}

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