{{Rsnum
|rsid=12431733
|Chromosome=14
|position=53824112
|Orientation=plus
|GMAF=0.3742
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 22.1 | 46.9 | 31.0
| HCB | 6.6 | 32.8 | 60.6
| JPT | 4.4 | 24.8 | 70.8
| YRI | 17.7 | 40.8 | 41.5
| ASW | 15.8 | 54.4 | 29.8
| CHB | 6.6 | 32.8 | 60.6
| CHD | 3.7 | 33.0 | 63.3
| GIH | 9.0 | 46.0 | 45.0
| LWK | 9.1 | 50.9 | 40.0
| MEX | 10.3 | 44.8 | 44.8
| MKK | 15.6 | 48.7 | 35.7
| TSI | 31.4 | 39.2 | 29.4
| 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=0.000003
|OR=1.13
|ORtxt=[NR]
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs12431733
|overall_frequency_n=50
|overall_frequency_d=128
|overall_frequency=0.390625
|n_genomes=36
|n_genomes_annotated=0
|n_haplomes=44
|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}}