{{Rsnum
|rsid=1768208
|Gene=MOBP
|Chromosome=3
|position=39481512
|Orientation=plus
|GMAF=0.3489
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=MOBP
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 51.8 | 37.5 | 10.7
| HCB | 12.9 | 39.4 | 47.7
| JPT | 17.0 | 46.4 | 36.6
| YRI | 99.3 | 0.7 | 0.0
| ASW | 80.7 | 19.3 | 0.0
| CHB | 12.9 | 39.4 | 47.7
| CHD | 20.6 | 40.2 | 39.3
| GIH | 35.7 | 50.0 | 14.3
| LWK | 97.1 | 2.9 | 0.0
| MEX | 28.6 | 41.1 | 30.4
| MKK | 87.5 | 12.5 | 0.0
| TSI | 50.0 | 40.0 | 10.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21685912
|Trait=None
|Title=Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.
|RiskAllele=
|Pval=5E-17
|OR=1.3700
|ORtxt=[1.28-1.49]
|OA=1
}}

{{PMID Auto
|PMID=23116876
|Title=An exploratory study on STX6, MOBP, MAPT, and EIF2AK3 and late-onset Alzheimer's disease.
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | Illumina Human 1M}}