{{Rsnum
|rsid=864643
|Gene=MOBP
|Chromosome=3
|position=39514089
|Orientation=minus
|GMAF=0.3085
|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 | 1.8 | 36.3 | 61.9
| HCB | 4.4 | 27.7 | 67.9
| JPT | 8.0 | 40.7 | 51.3
| YRI | 38.8 | 42.9 | 18.4
| ASW | 28.6 | 55.4 | 16.1
| CHB | 4.4 | 27.7 | 67.9
| CHD | 8.3 | 33.9 | 57.8
| GIH | 0.0 | 22.8 | 77.2
| LWK | 43.6 | 45.5 | 10.9
| MEX | 12.1 | 34.5 | 53.4
| MKK | 25.0 | 57.1 | 17.9
| TSI | 6.9 | 39.2 | 53.9
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=18839057
|Trait=Attention-deficit/hyperactivity disorder
|Title=Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies
|RiskAllele=
|Pval=1E-8
|OR=NR
|ORtxt=NR
}}

{{PMID Auto
|PMID=17357082
|Title=Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms.
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs864643
|overall_frequency_n=43
|overall_frequency_d=128
|overall_frequency=0.335938
|n_genomes=32
|n_genomes_annotated=0
|n_haplomes=43
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

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