{{Rsnum
|rsid=12185268
|Gene=IMP5
|Chromosome=17
|position=45846317
|Orientation=plus
|GMAF=0.1162
|Gene_s=MAPT-AS1,SPPL2C
|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 | 60.2 | 38.9 | 0.9
| HCB | 100.0 | 0.0 | 0.0
| JPT | 99.1 | 0.9 | 0.0
| YRI | 100.0 | 0.0 | 0.0
| ASW | 82.5 | 17.5 | 0.0
| CHB | 100.0 | 0.0 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 82.2 | 16.8 | 1.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 70.7 | 22.4 | 6.9
| MKK | 89.1 | 8.3 | 2.6
| TSI | 42.2 | 44.1 | 13.7
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21738487
|Trait=None
|Title=Web-based genome-wide association study identifies two novel Loci and a substantial genetic component for Parkinson's disease.
|RiskAllele=A
|Pval=3E-14
|OR=1.3000
|ORtxt=[1.22-1.39]
|OA=1
}}

{{PMID Auto
|PMID=18985386
|Title=Genomewide association study for susceptibility genes contributing to familial Parkinson disease.
|OA=1
}}

{{PMID Auto
|PMID=20070850
|Title=Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease.
|OA=1
}}

{{GET Evidence
|gene=NM_175882
|aa_change=Ile471Val
|aa_change_short=I471V
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs12185268
|overall_frequency_n=11
|overall_frequency_d=122
|overall_frequency=0.0901639
|n_genomes=5
|n_genomes_annotated=0
|n_haplomes=7
|n_articles=0
|n_articles_annotated=0
|pph2_score=0.006
|nblosum100=-4
|autoscore=0
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}