{{Rsnum
|rsid=1994090
|Gene=SLC2A13
|Chromosome=12
|position=40034759
|Orientation=plus
|GMAF=0.135
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=SLC2A13
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 7.1 | 32.7 | 60.2
| HCB | 0.0 | 13.9 | 86.1
| JPT | 0.9 | 8.9 | 90.2
| YRI | 1.4 | 10.2 | 88.4
| ASW | 0.0 | 12.3 | 87.7
| CHB | 0.0 | 13.9 | 86.1
| CHD | 0.0 | 11.9 | 88.1
| GIH | 6.0 | 39.0 | 55.0
| LWK | 0.9 | 14.5 | 84.5
| MEX | 0.0 | 15.5 | 84.5
| MKK | 1.9 | 15.5 | 82.6
| TSI | 7.8 | 31.4 | 60.8
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=19915576
|Trait=Parkinson's disease
|Title=Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease
|RiskAllele=G
|Pval=3E-8
|OR=1.39
|ORtxt=[1.24-1.56]
}}

{{PMID Auto
|PMID=20413655
|Title=Genetics of neurodegenerative diseases: insights from high-throughput resequencing.
|OA=1
}}

{{PMID Auto
|PMID=21268244
|Title=Association of GWAS loci with PD in China.
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1994090
|overall_frequency_n=116
|overall_frequency_d=128
|overall_frequency=0.90625
|n_genomes=55
|n_genomes_annotated=0
|n_haplomes=99
|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 | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}