{{Rsnum
|rsid=17115100
|Gene=CYP17A1
|Chromosome=10
|position=104591393
|Orientation=plus
|GMAF=0.1593
|Gene_s=CYP17A1,CYP17A1-AS1
|Assembly=GRCh37.p5
|GenomeBuild=37.3
|dbSNPBuild=137
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}
{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 85.0 | 14.2 | 0.9
| HCB | 41.6 | 41.6 | 16.8
| JPT | 44.2 | 43.4 | 12.4
| YRI | 93.2 | 6.8 | 0.0
| ASW | 89.5 | 10.5 | 0.0
| CHB | 41.6 | 41.6 | 16.8
| CHD | 41.7 | 46.3 | 12.0
| GIH | 51.5 | 40.6 | 7.9
| LWK | 90.9 | 9.1 | 0.0
| MEX | 63.8 | 31.0 | 5.2
| MKK | 89.0 | 11.0 | 0.0
| TSI | 77.5 | 21.6 | 1.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=19915575
|Trait=Parkinson's disease
|Title=Genome-wide association study reveals genetic risk underlying Parkinson's disease
|RiskAllele=T
|Pval=7E-8
|OR=1.25
|ORtxt=[NR]
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs17115100
|overall_frequency_n=887
|overall_frequency_d=10758
|overall_frequency=0.0824503
|n_genomes=5
|n_genomes_annotated=0
|n_haplomes=5
|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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}