{{Rsnum
|rsid=1805874
|Gene=CALB1
|Chromosome=8
|position=90069834
|Orientation=plus
|GMAF=0.4357
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=CALB1
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 9.7 | 40.7 | 49.6
| HCB | 47.4 | 46.7 | 5.8
| JPT | 58.4 | 34.5 | 7.1
| YRI | 4.1 | 27.2 | 68.7
| ASW | 1.8 | 50.9 | 47.4
| CHB | 47.4 | 46.7 | 5.8
| CHD | 34.9 | 52.3 | 12.8
| GIH | 25.7 | 45.5 | 28.7
| LWK | 3.6 | 44.5 | 51.8
| MEX | 37.9 | 34.5 | 27.6
| MKK | 15.4 | 39.1 | 45.5
| TSI | 8.8 | 42.2 | 49.0
| HapMapRevision=28
}}{{PMID|18568448}} Parkinson's disease (PD). [[rs1805874]] showed significance in both analyses (P = 7.1 x 10(-5); recessive model).

However, a more recent study of 4 Caucasian populations (comprising 1500+ patients) found no association between [[rs1805874]] and [[Parkinson's disease]], at least for these populations.{{PMID|19674066}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}