{{Rsnum
|rsid=393152
|Gene=C17orf69
|Chromosome=17
|position=45641777
|Orientation=plus
|GMAF=0.2369
|Gene_s=CRHR1,C17orf69
|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 | 59.3 | 39.8 | 0.9
| HCB | 100.0 | 0.0 | 0.0
| JPT | 99.1 | 0.9 | 0.0
| YRI | 15.6 | 40.1 | 44.2
| ASW | 26.3 | 42.1 | 31.6
| CHB | 100.0 | 0.0 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 82.2 | 16.8 | 1.0
| LWK | 33.6 | 49.1 | 17.3
| MEX | 63.8 | 27.6 | 8.6
| MKK | 41.0 | 44.9 | 14.1
| TSI | 41.2 | 45.1 | 13.7
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=19915575
|Trait=Parkinson's disease
|Title=Genome-wide association study reveals genetic risk underlying Parkinson's disease
|RiskAllele=G
|Pval=2E-16
|OR=1.30
|ORtxt=[NR]
|OA=1
}}

{{omim
|id=600274
|rsnum=393152
}}

{{omim
|id=613164
|rsnum=393152
}}

{{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
}}

{{PMID Auto
|PMID=21898123
|Title=The age at motor symptoms onset in LRRK2-associated Parkinson's disease is affected by a variation in the MAPT locus: a possible interaction.
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs393152
|overall_frequency_n=41
|overall_frequency_d=126
|overall_frequency=0.325397
|n_genomes=28
|n_genomes_annotated=0
|n_haplomes=38
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

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